Cms 847 Template

Cms 847 Template

The CMS 847 form is a Certificate of Medical Necessity specifically designed for osteogenesis stimulators, a type of durable medical equipment. This form is essential for healthcare providers to certify that a patient's use of these devices is medically necessary, ensuring that Medicare can process claims appropriately. Understanding how to accurately complete this form is crucial for both patients and providers to facilitate the necessary care.

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Table of Contents

The CMS 847 form, officially known as the Certificate of Medical Necessity for Osteogenesis Stimulators, plays a crucial role in the healthcare system, particularly for patients requiring specific durable medical equipment. This form is essential for documenting the medical necessity of osteogenesis stimulators, which are devices used to promote bone healing. It includes several sections that gather vital patient information, such as the patient's name, Medicare ID, and the supplier's details. The form also requires the treating physician to certify the necessity of the device based on clinical assessments. Notably, Section B collects specific clinical information that helps determine the medical necessity for the equipment, including diagnosis codes and responses to pertinent questions regarding the patient's condition. Additionally, the form mandates a narrative description of the equipment and its costs, ensuring transparency and compliance with Medicare regulations. The physician's signature at the end attests to the accuracy of the information provided, reinforcing the importance of proper documentation in securing necessary treatments for patients.

Cms 847 Sample

CERTIFICATE OF MEDICAL NECESSITY
CMS-847 — OSTEOGENESIS STIMULATORS
SECTION A: Certification Type/Date: INITIAL ___/___/___ D ___/___/___ RECERTIFICATION___/___/___
PATIENT NAME, ADDRESS, TELEPHONE and MEDICARE ID
REVISE
SUPPLIER NAME, ADDRESS, TELEPHONE and NSC or NPI #
(__ __ __) __ __ __ – __ __ __ __ Medicare ID
(__ __ __) __ __ __ –__ __ __ __ NSC or NPI #____________
PLACE OF SERVICE ______________ Supply Item/Service/Procedure Code(s): PT DOB ____/____/____ Sex ____ (M/F) Ht. ____(in) Wt ____
NAME and ADDRESS of FACILITY
(__ __ __) __ __ __ – __ __ __ __ UPIN or NPI #____
PHYSICIAN NAME, ADDRESS, TELEPHONE and UPIN or NPI #
if applicable (see reverse)
________
SECTION B: Information in this Section May Not Be Completed by the Supplier of the Items/Supplies.
EST. LENGTH OF NEED (# OF MONTHS): ______ 1–99 (99=LIFETIME) DIAGNOSIS CODES: ______ ______ ______ ______
ANSWERS QUESTIONS 1–5 ARE BLANK.
ANSWER QUESTIONS 6–8 FOR NONSPINAL ELECTRICAL OSTEOGENESIS STIMULATOR.
ANSWER QUESTIONS 9–11 FOR SPINAL ELECTRICAL OSTEOGENESIS STIMULATOR.
ANSWER QUESTIONS 6 AND 12 FOR ULTRASONIC OSTEOGENSIS STIMULATOR.
(Check Y for Yes, N for No, or D for Does Not Apply. For questions about months, enter 1–99 or D. If less than one month, enter 1.)
a) oY o N oD
a) oY o N oD
(b
b )____________
o Y o N o
_
D
a) oY o N oD
b)
a) o Y o N o
b)_____________
c)______________
6. In a fracture, has there been no clinically significant radiographic evidence of healing for a minimum of 90 days?
7. (a) Does the patient have a failed fusion of a joint other than the spine?
) How many months prior to ordering the device did the patient have the fusion?
8. Does the patient have a congenital pseudoarthrosis?
9. (a) Is the device being ordered as a treatment of a failed single level spinal fusion surgery in a patient who has
not had a recent repeat fusion?
(b) How many months prior to ordering the device did the patient have the fusion?
D 10. (a) Is the device being ordered as an adjunct to repeat single level spinal fusion surgery in a patient with a
previously failed spinal fusion at the same level(s)?
(b) How many months prior to ordering the device did the patient have the repeat fusion?
(c) How many months prior to ordering the device did the patient have the previously failed fusion?
o Y o N o D
o Y o N o D
11. Is the device being ordered following multi¬level spinal fusion surgery?
12. Has there been at least one open surgical intervention for treatment of the fracture?
NAME OF PERSON ANSWERING SECTION B QUESTIONS, IF OTHER THAN PHYSICIAN (Please Print):
NAME__________________________________ TITLE________________________EMPLOYER________________________
SECTION C: Narrative Description of Equipment and Cost
(1) Narrative description of Iall items, accessories and option ordered; (2) Suppliers charge; and (3) Medicare Fee Schedule Allowance for
each item, accessory, and option (see instructions on back)
SECTION D: PHYSICIAN Attestation and Signature/Date
I certify that I am the treating physician identified in Section A of this form. I have received Sections A, B and C of the Certificate of
Medical Necessity (including charges for items ordered). Any statement on my letterhead attached hereto, has been reviewed and signed
by me. I certify that the medical necessity information in Section B is true, accurate and complete, to the best of my knowledge, and I
understand that any falsification, omission, or concealment of material fact in that section may subject me to civil or criminal liability.
PHYSICIAN’S SIGNATURE_________________________________________________________DATE _____/_____/_____
Signature and Date Stamps Are Not Acceptable.
Form CMS–847 (06/19)
DEPARTMENT OF HEALTH AND HUMAN SERVICES
CENTERS FOR MEDICARE & MEDICAID SERVICES
Form Approved OMB
No. 0938-0679
Expires 02/2024
DME 04.04C
SECTION A:
CERTIFICATION
DATE:
PATIENT
INFORMATION:
SUPPLIER
INFORMATION:
PLACE OF SERVICE:
FACILITY NAME:
SUPPLY ITEM/SERVICE
PROCEDURE CODE(S):
PATIENT DOB, HEIGHT,
WEIGHT AND SEX:
PHYSICIAN NAME,
ADDRESS:
PHYSICIAN
INFORMATION:
PHYSICIAN’S
TELEPHONE NO:
SECTION B:
EST. LENGTH OF NEED:
DIAGNOSIS CODES:
QUESTION SECTION:
NAME OF PERSON
ANSWERING SECTION B
QUESTIONS:
SECTION C:
NARRATIVE
DESCRIPTION OF
EQUIPMENT & COST:
SECTION D:
PHYSICIAN
ATTESTATION:
PHYSICIAN SIGNATURE
AND DATE:
(May be completed by the supplier)
If this is an initial certification for this patient, indicate this by placing date (MM/DD/YY) needed initially in the space TYPE/
marked “INITIAL.” If this is a revised certification (to be completed when the physician changes the order, based on the
patient’s changing clinical needs), indicate the initial date needed in the space marked “INITIAL,” and indicate the
recertification date in the space marked “REVISED.” If this is a recertification, indicate the initial date needed in the
space marked “INITIAL,” and indicate the recertification date in the space marked “RECERTIFICATION.” Whether
submitting a REVISED or a RECERTIFIED CMN, be sure to always furnish the INITIAL date as well as the REVISED or
RECERTIFICATION date.
Indicate the patient’s name, permanent legal address, telephone number and his/her Medicare ID as it appears on his/her
Medicare card and on the claim form.
Indicate the name of your company (supplier name), address and telephone number along with the Medicare Supplier
Number assigned to you by the National Supplier Clearinghouse (NSC) or applicable National Provider Identifier (NPI). If
using the NPI Number, indicate this by using the qualifier XX followed by the 10-digit number. If using a legacy number,
e.g. NSC number, use the qualifier 1C followed by the 10-digit number. (For example. 1Cxxxxxxxxxx)
Indicate the place in which the item is being used, i.e., patient’s home is 12, skilled nursing facility (SNF) is 31, End
Stage Renal Disease (ESRD) facility is 65, etc. Refer to the DMERC supplier manual for a complete list.
If the place of service is a facility, indicate the name and complete address of the facility.
List all procedure codes for items ordered. Procedure codes that do not require certification should not be listed
on the CMN.
Indicate patient’s date of birth (MM/DD/YY) and sex (male or female); height in inches and weight in pounds, if requested.
Indicate the PHYSICIAN’S name and complete mailing address.
Accurately indicate the treating physician’s Unique Physician Identification Number (UPIN) or applicable National
Provider Identifier (NPI). If using the NPI Number, indicate this by using the qualifier XX followed by the 10-digit number.
If using UPIN number, use the qualifier 1G followed by the 6-digit number. (For example. 1Gxxxxxx)
Indicate the telephone number where the physician can be contacted (preferably where records would be accessible
pertaining to this patient) if more information is needed.
(May not be completed by the supplier. While this section may be completed by a non-physician clinician, or a
Physician employee, it must be reviewed, and the CMN signed (in Section D) by the treating practitioner.)
Indicate the estimated length of need (the length of time the physician expects the patient to require use of the ordered
item) by filling in the appropriate number of months. If the patient will require the item for the duration of his/her life,
then enter “99”.
In the first space, list the diagnosis code that represents the primary reason for ordering this item. List any additional
diagnosis codes that would further describe the medical need for the item (up to 4 codes).
This section is used to gather clinical information to help Medicare determine the medical necessity for the item(s)
being ordered. Answer each question which applies to the items ordered, checking “Y” for yes, “N” for no, or “D” for
does not apply.
If a clinical professional other than the treating physician (e.g., home health nurse, physical therapist, dietician) or a
physician employee answers the questions of Section B, he/she must print his/her name, give his/her professional title
and the name of his/her employer where indicated. If the physician is answering the questions, this space may be
left blank.
(To be completed by the supplier)
Supplier gives (1) a narrative description of the item(s) ordered, as well as all options, accessories, supplies and drugs;
(2) the supplier’s charge for each item(s), options, accessories, supplies and drugs; and (3) the Medicare fee schedule
allowance for each item(s), options, accessories, supplies and drugs, if applicable.
(To be completed by the physician)
The physician’s signature certifies (1) the CMN which he/she is reviewing includes Sections A, B, C and D; (2) the
answers in Section B are correct; and (3) the self-identifying information in Section A is correct.
After completion and/or review by the physician of Sections A, B and C, the physician’s must sign and date the CMN in
Section D, verifying the Attestation appearing in this Section. The physician’s signature also certifies the items ordered
are medically necessary for this patient.
INSTRUCTIONS FOR COMPLETING THE CERTIFICATE OF MEDICAL NECESSITY
FOR OSTEOGENESIS STIMULATORS
Form CMS-847 (06/19) INSTRUCTIONS
According to the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for
this information collection is 0938-0679. The time required to complete this information collection is estimated to average 12 minutes per response, including the time to review instructions, search existing
resources, gather the data needed, and complete and review the information collection. If you have any comments concerning the accuracy of the time estimate or suggestions for improving this form,
please write to: CMS, Attn: PRA Reports Clearance Officer, 7500 Security Blvd. Baltimore, Maryland 21244.
DO NOT SUBMIT CLAIMS TO THIS ADDRESS. Please see http://www.medicare.gov/ for information on claim filing.

Document Attributes

Fact Name Description
Form Purpose The CMS-847 form is used to certify medical necessity for osteogenesis stimulators, which are devices that assist in the healing of bone fractures.
Certification Types Three types of certifications can be indicated: Initial, Revised, and Recertification. Each type requires specific dates to be filled out.
Section B Restrictions Section B must not be completed by the supplier. It is designated for clinical professionals or the treating physician to provide necessary medical information.
Length of Need The estimated length of need for the device can range from 1 to 99 months, with 99 indicating a lifetime requirement.
Governing Law This form is governed by federal Medicare regulations, specifically under the Department of Health and Human Services.
Physician's Attestation The physician must sign and date Section D, certifying the accuracy of the information provided and the medical necessity of the items ordered.

Cms 847: Usage Instruction

Completing the CMS 847 form is a crucial step in ensuring that medical necessity is documented for osteogenesis stimulators. This form requires accurate information about the patient, the supplier, and the physician, as well as specific clinical details. Follow the steps below to fill out the form correctly.

  1. Section A: Certification Type/Date
    • Select the appropriate certification type: INITIAL, REVISED, or RECERTIFICATION.
    • Fill in the date (MM/DD/YYYY) for the selected certification type.
    • Provide the patient’s name, address, telephone number, and Medicare ID.
    • Enter the supplier’s name, address, telephone number, and either the NSC or NPI number.
    • Indicate the place of service.
    • List the supply item/service/procedure code(s).
    • Fill in the patient’s date of birth, sex, height, and weight.
    • Provide the name and address of the facility, if applicable.
    • Include the physician’s name, address, telephone number, and UPIN or NPI number.
  2. Section B: Information
    • Do not complete this section if you are the supplier. It must be filled out by a clinician.
    • Indicate the estimated length of need in months (1-99, with 99 representing lifetime).
    • List the relevant diagnosis codes (up to four).
    • Answer questions 1-11 as applicable by checking Y (Yes), N (No), or D (Does Not Apply).
    • If someone other than the physician answers these questions, provide their name, title, and employer.
  3. Section C: Narrative Description of Equipment and Cost
    • Provide a narrative description of all items, accessories, and options ordered.
    • List the supplier’s charge for each item.
    • Include the Medicare Fee Schedule Allowance for each item.
  4. Section D: Physician Attestation and Signature/Date
    • The physician must review Sections A, B, and C.
    • Sign and date the form in the designated area.
    • Ensure that the signature is handwritten; stamped signatures are not acceptable.

Frequently Asked Questions

  1. What is the CMS-847 form?

    The CMS-847 form, also known as the Certificate of Medical Necessity for Osteogenesis Stimulators, is a document required by Medicare to establish the medical necessity for certain durable medical equipment (DME). This form is particularly focused on osteogenesis stimulators, which are devices used to promote bone healing.

  2. Who needs to complete the CMS-847 form?

    The form must be completed by the treating physician, although some sections may be filled out by a non-physician clinician or a physician employee. However, the physician must review and sign the form to certify that the information is accurate and complete.

  3. What information is required in Section A of the CMS-847?

    Section A requires details about the patient and the supplier. This includes:

    • Patient's name, address, telephone number, and Medicare ID.
    • Supplier's name, address, telephone number, and National Supplier Clearinghouse (NSC) or National Provider Identifier (NPI) number.
    • Place of service where the equipment will be used.
    • Supply item/service/procedure codes.
  4. What is the purpose of Section B?

    Section B gathers clinical information to determine the medical necessity of the osteogenesis stimulator. It includes questions that must be answered based on the patient's condition. This section may not be completed by the supplier and requires careful consideration by the physician or qualified clinician.

  5. How does a physician certify the information on the CMS-847?

    In Section D, the physician must sign and date the form, certifying that they have reviewed Sections A, B, and C. By signing, the physician confirms that the information provided is true and that the items ordered are medically necessary for the patient.

  6. What happens if the CMS-847 form is not completed correctly?

    If the form is not completed accurately, it may lead to delays in obtaining the necessary equipment or even denial of coverage by Medicare. It is crucial to ensure all sections are filled out completely and correctly to avoid complications.

  7. How long is the CMS-847 form valid?

    The CMS-847 form is valid for the duration specified in the estimated length of need section. This can range from one month to a lifetime (indicated by "99"). If the patient's needs change, a revised or recertified form may be required.

Common mistakes

Completing the CMS 847 form accurately is essential for ensuring that patients receive the necessary medical equipment. However, several common mistakes can hinder this process. One prevalent error occurs when individuals neglect to fill out the Certification Type/Date section properly. This section requires specific dates for initial, revised, or recertification requests. Omitting or incorrectly marking these dates can lead to delays in processing.

Another frequent mistake involves the patient information section. Failing to provide the correct Medicare ID, name, or address can result in complications. It is crucial that this information matches what is on the patient’s Medicare card. Any discrepancies may lead to claim denials or delays in equipment provision.

In Section B, individuals sometimes leave questions unanswered. This section is critical as it gathers clinical information to establish medical necessity. Not answering questions or providing incomplete responses can trigger additional requests for information from Medicare, prolonging the approval process.

Additionally, some individuals mistakenly believe that Section B can be completed by the supplier. This section must be filled out by a qualified clinician, such as a physician or a healthcare professional working under their supervision. Misunderstanding this requirement can lead to invalid submissions.

Another common error arises in the diagnosis codes section. Entering incorrect or outdated codes can misrepresent the medical necessity of the equipment. It is vital to ensure that the codes accurately reflect the patient’s condition and align with the items being requested.

People often overlook the importance of the narrative description in Section C. Failing to provide a clear and detailed description of the equipment, along with associated costs, can result in confusion and further inquiries from Medicare. This section should comprehensively outline all items and their purposes.

Signature requirements in Section D are also a frequent stumbling block. Some individuals may use a signature stamp, which is not acceptable. The physician must personally sign and date the form to validate the information provided, ensuring compliance with Medicare guidelines.

Lastly, a lack of attention to the place of service can create issues. Incorrectly indicating where the item will be used may lead to complications in reimbursement. It is important to accurately represent the setting, whether it is a home, hospital, or skilled nursing facility.

Documents used along the form

The CMS-847 form, also known as the Certificate of Medical Necessity for Osteogenesis Stimulators, is crucial for ensuring that patients receive the necessary medical equipment. In addition to this form, there are several other documents that may be required to support the process. Below are some of these forms and documents, along with a brief description of each.

  • CMS-1500 Form: This is a standard claim form used by healthcare providers to bill Medicare and other insurance carriers for services rendered. It includes patient information, provider details, and the services provided.
  • Physician's Order: This document is a formal request from a physician to provide specific medical services or equipment to a patient. It outlines the medical necessity and the specific items needed for treatment.
  • Patient Medical Records: These records contain the patient's medical history, treatment plans, and any relevant diagnostic information. They help substantiate the medical necessity for the equipment being requested.
  • Medicare Coverage Guidelines: This document outlines the specific criteria that must be met for Medicare to cover certain medical devices or treatments. It serves as a reference for both providers and patients regarding coverage eligibility.

Having these documents prepared and organized can significantly streamline the process of obtaining necessary medical equipment. It is essential to ensure that all information is accurate and complete to avoid any delays in care.

Similar forms

The CMS-847 form, which is a Certificate of Medical Necessity for osteogenesis stimulators, shares similarities with several other important documents used in the healthcare and insurance sectors. Below is a list of six documents that are comparable to the CMS-847, along with explanations of their similarities:

  • CMS-1500 Form: This is a standard claim form used by healthcare providers to bill Medicare and other insurers. Like the CMS-847, it requires detailed patient and provider information, as well as diagnosis codes to justify medical necessity.
  • CMS-484 Form: This form is used for home health services and includes information about the patient's condition and the services required. Both forms emphasize the need for medical necessity documentation to ensure coverage.
  • CMS-22 Form: Known as the "Request for Medicare Payment," this form is used to request reimbursement for services rendered. Similar to the CMS-847, it requires specific details about the patient and the services provided to validate the claim.
  • Prior Authorization Request Form: This form is submitted to insurance companies to obtain approval for specific treatments or services. Both the prior authorization request and the CMS-847 require comprehensive medical justification to confirm that the treatment is necessary.
  • Certificate of Medical Necessity (CMN) for Durable Medical Equipment: This document is specifically for other types of durable medical equipment. It shares the same purpose as the CMS-847, which is to certify the medical necessity of the equipment for the patient’s treatment.
  • Patient Assessment Form: Used in various healthcare settings, this form gathers information about a patient's health status and treatment needs. Like the CMS-847, it is crucial for determining the appropriateness of care and ensuring that services align with the patient's medical needs.

Each of these documents plays a vital role in ensuring that healthcare providers can effectively communicate the necessity of services and equipment to insurance companies, ultimately supporting patient care.

Dos and Don'ts

When filling out the CMS 847 form, it is important to follow specific guidelines to ensure accuracy and compliance. Below is a list of things to do and avoid.

  • Do provide accurate patient information, including the patient's name, address, and Medicare ID.
  • Do clearly indicate the type of certification: initial, revised, or recertification.
  • Do ensure that all required sections are completed, especially those that pertain to medical necessity.
  • Do include the estimated length of need in months, using 1-99 or indicating lifetime need with "99."
  • Do have the physician review and sign the form in Section D, certifying the information provided.
  • Don't leave any questions in Section B unanswered; provide responses for all applicable questions.
  • Don't submit claims without ensuring that all information is accurate and complete, as this may lead to delays or denials.

Misconceptions

Understanding the CMS 847 form, also known as the Certificate of Medical Necessity for Osteogenesis Stimulators, can be challenging. Here are five common misconceptions about this form:

  • The CMS 847 form is only for spinal osteogenesis stimulators. This is incorrect. While it includes sections for spinal stimulators, it also addresses non-spinal electrical and ultrasonic osteogenesis stimulators. Each type has specific questions that must be answered to establish medical necessity.
  • Only physicians can fill out the entire form. This is a misconception. Although the form must be signed by a physician, certain sections can be completed by other healthcare professionals, such as a physical therapist or a nurse. However, these sections must be reviewed and signed by the treating physician.
  • Once the CMS 847 form is submitted, it cannot be revised. This is not true. The form can be revised if the physician changes the order based on the patient's evolving clinical needs. It is essential to indicate both the initial and revised dates on the form.
  • The form is not necessary if the patient has a Medicare Advantage plan. This is misleading. Even patients with Medicare Advantage plans may require the CMS 847 form to document medical necessity for coverage of osteogenesis stimulators. Each plan may have its specific requirements, but the form serves as a critical piece of documentation.
  • Completing the form guarantees approval for coverage. This is a common misunderstanding. While the CMS 847 form is a vital step in the process, approval for coverage ultimately depends on Medicare's assessment of medical necessity based on the information provided in the form.

Key takeaways

Filling out the CMS 847 form requires careful attention to detail to ensure compliance with Medicare requirements. Below are key takeaways regarding the form's use and completion:

  • Certification Types: The form allows for initial certifications, revisions, and recertifications. It is essential to indicate the appropriate type and dates clearly.
  • Patient Information: Accurate patient details, including name, address, telephone number, and Medicare ID, must be provided to avoid processing delays.
  • Section B Restrictions: This section, which gathers clinical information to establish medical necessity, cannot be completed by the supplier. A physician or qualified clinical professional must review and sign it.
  • Narrative Description: Section C requires a detailed narrative description of the equipment, including costs and Medicare fee schedule allowances. This information is critical for reimbursement.
  • Physician Attestation: The physician's signature in Section D certifies that the information provided is accurate and complete. This step is crucial, as any inaccuracies may lead to legal implications.