Identity
- Trade Name
- PLR HIP SYSTEM FDA UDI
- Generic Name
- Revision uncoated femoral stem prosthesis FDA UDI
- Model / Reference
- 11-158323 FDA UDI
Identifiers
- Catalog Number
- 11-158323 FDA UDI
- Primary DI / UDI-DI
- 00880304208339 FDA UDI
- 510(k) Number
- K994184 FDA UDI
- FDA Product Code
- JDI FDA UDILZO FDA UDI
- GMDN Term
- Revision uncoated femoral stem prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3350 FDA UDI888.3353 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Revision uncoated femoral stem prosthesis
Plr Hip System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Revision uncoated femoral stem prosthesis.
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- Pantheon System — ADLER ORTHO SPA · Class II
- Pantheon System — ADLER ORTHO SPA · Class II
- Pantheon System — ADLER ORTHO SPA · Class II
- Pantheon System — ADLER ORTHO SPA · Class II
- REVISION — Limacorporate · Class II
- Pantheon System — ADLER ORTHO SPA · Class II
- REVISION — Limacorporate · Class II
Cleared under the same submission
K994184 also covers:
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
- PLR HIP SYSTEM — Biomet Orthopedics, Inc.
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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI aad67782-ded9-42ea-a2d7-2406436d276c 36 fields · synced Jun 8, 2026