Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System
K242831 is the FDA 510(k) clearance record for Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System, a class II device, cleared for Howmedica Osteonics Corp., Dba Stryker Orthopaedics on under FDA product code JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer). FDA records list 33 510(k) clearances for Howmedica Osteonics Corp., Dba Stryker Orthopaedics, from to . As of , FDA records show no recalls naming K242831.
Clearance record
- Decision date
- Received
- (76 days to decision)
- Product code
- JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- Regulation
- 21 CFR 888.3560
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Howmedica Osteonics Corp., Dba Stryker Orthopaedics 325 Corporate Dr., Mahwah NJ
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code JWH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 1 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 1 |
| July 2026 | 2 |
| August 2026 | 1 |
| September 2026 | 6 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
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