OSS-BODIES PROXIMAL TIBIAL SLEEVE
FDA 510(k) clearance K060131 · decided 2006-02-15
Clearance details
- K-number
- K060131
- Device name
- OSS-BODIES PROXIMAL TIBIAL SLEEVE
- Applicant
- Biomet Manufacturing Corp
- Decision
- Substantially Equivalent
- Date received
- 2006-01-18
- Decision date
- 2006-02-15
- Days to decision
- 28 days
- Clearance type
- Special
- Product code
- KRO
- Device class
- 2
- Regulation number
- 888.3510
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Warsaw, IN, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| Oxford Partial Knee System (P010014/S117) | Biomet Manufacturing Corp | 2026-07-13 |
| Oxford Partial Knee System; Cementless OxfordPartial Knee System (P010014/S112) | Biomet Manufacturing Corp | 2026-05-27 |
| Oxford® Partial Knee System (P010014/S116) | Biomet Manufacturing Corp | 2026-05-12 |
| Oxford® Partial Knee System (P010014/S115) | Biomet Manufacturing Corp | 2026-04-20 |
| Oxford Cementless Partial Knee System (P010014/S114) | Biomet Manufacturing Corp | 2026-03-06 |
| Oxford Partial Knee System (P010014/S113) | Biomet Manufacturing Corp | 2026-01-16 |
| Oxford Knee System (P010014/S111) | Biomet Manufacturing Corp | 2025-08-07 |
| Oxford Partial Knee System (P010014/S109) | Biomet Manufacturing Corp | 2025-08-07 |