Identity
- Trade Name
- MRS FDA UDI
- Generic Name
- Coated shoulder humeral stem prosthesis FDA UDI
- Device Name
- Humeral Module FDA UDI
- Model / Reference
- 6487-1-120 FDA UDI
- Description
- Humeral Module FDA UDI
Identifiers
- Catalog Number
- 6487-1-120 FDA UDI
- Primary DI / UDI-DI
- 07613327048988 FDA UDI
- 510(k) Number
- K954559 FDA UDI
- FDA Product Code
- HSD FDA UDI
- GMDN Term
- Coated shoulder humeral stem prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3690 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
Category: Coated shoulder humeral stem prosthesis
Mrs by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coated shoulder humeral stem prosthesis.
- OsseoFit™ Stemless Shoulder — Zimmer, Inc. · Class II
- TORNIER PERFORM™ HUMERAL SYSTEM — TORNIER, INC. · Class II
- Tornier HRS — TORNIER, INC. · Class II
- Comprehensive® Shoulder System — Biomet Orthopedics, Inc. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class II
- Comprehensive SRS — Biomet Orthopedics, Inc. · Class II
- INHANCE — DEPUY (IRELAND) · Class II
- Aequalis™ PerFORM+ — TORNIER, INC. · Class II
Cleared under the same submission
K954559 also covers:
- 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.
- 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Howmedica Osteonics Corp.
Sources (1)
- FDA UDI bc851320-d3a8-4306-b9b8-29475d0eb8b7 35 fields · synced Jun 8, 2026