Identity
- Trade Name
- DJO SURGICAL FDA UDI
- Generic Name
- Cruciate-retaining total knee prosthesis FDA UDI
- Device Name
- PATELLA,METAL BACKED 29MM W/NS BEADS FDA UDI
- Model / Reference
- 110-02-029 FDA UDI
- Description
- PATELLA,METAL BACKED 29MM W/NS BEADS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888912108263 FDA UDI
- 510(k) Number
- K932246 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Cruciate-retaining total knee prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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: Cruciate-retaining total knee prosthesisMetal-backed patella prosthesis
Djo Surgical by Encore Medical, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metal-backed patella prosthesis.
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- Triathlon — Howmedica Osteonics Corp. · Class II
- Triathlon — Howmedica Osteonics Corp. · Class II
- LCS COMPLETE — DEPUY ORTHOPAEDICS, INC. · Class III
- NEXGEN® TRABECULAR METAL® — Zimmer, Inc. · Class II
Cleared under the same submission
K932246 also covers:
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
- Encore Medical, L.p.
Sources (1)
- FDA UDI 2d09dc04-24b4-47c7-bc35-4fe3742a090a 34 fields · synced May 30, 2026