Ortho Development Corp.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories4
Latest Approval2025-12-19
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K253161 | Balanced Knee System TriMax Porous Femoral Components | MBH | 2025-12-19 | View |
| 510(k) | K251052 | Trivicta® Hip Stem | MEH | 2025-05-22 | View |
| 510(k) | K242984 | BKS Revision System | JWH | 2024-10-25 | View |
| 510(k) | K242833 | Legend® Acetabular Shell | LPH | 2024-10-11 | View |
| 510(k) | K233758 | Trivicta Hip Stem | MEH | 2024-03-08 | View |
No matching devices.