Identity
- Trade Name
- MRS FDA UDI
- Generic Name
- Coated femoral stem prosthesis, modular FDA UDI
- Device Name
- Femoral Intercalary Stem FDA UDI
- Model / Reference
- 6485-3-217 FDA UDI
- Description
- Femoral Intercalary Stem FDA UDI
Identifiers
- Catalog Number
- 6485-3-217 FDA UDI
- Primary DI / UDI-DI
- 07613327048407 FDA UDI
- 510(k) Number
- K952970 FDA UDI
- FDA Product Code
- JDI FDA UDIKRO FDA UDI
- GMDN Term
- Coated femoral stem prosthesis, modular FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3350 FDA UDI888.3510 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 127.0 Millimeter FDA UDI
Category: Coated femoral stem prosthesis, modular
Mrs by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coated femoral stem prosthesis, modular.
- MALLORY/HEAD CALCAR HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- TheRay Collared and Collarless Femoral Stem — Nextstep Arthropedix · Class II
- STERIZO Total Hip System — CPM Medical Consultants, LLC · Class II
- PROFEMUR® — MicroPort Orthopedics Inc. · Class II
- MALLORY/HEAD CALCAR HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- Alteon — Exactech, Inc. · Class II
- ANTHOLOGY — Smith & Nephew, Inc. · Class III
- TheRay Collared and Collarless Femoral Stem — Nextstep Arthropedix · Class II
Cleared under the same submission
K952970 also covers:
- Kinematic — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
- MRS — Howmedica Osteonics Corp.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Howmedica Osteonics Corp.
Sources (1)
- FDA UDI baaf0371-c3c7-43f5-a4ef-0a74754f7661 36 fields · synced May 30, 2026