Metagen, LLC
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K983976 | METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM | JDQ | 1998-12-30 | View |
| 510(k) | K980609 | SEGMENTAL DEFECT REPLACEMENT SYSTEM | HSB | 1998-05-18 | View |
| 510(k) | K980020 | ACTIVELOCK MODULAR FEMORAL HIP SYSTEM | LPH | 1998-04-03 | View |
| 510(k) | K964003 | METAGEN ALL POLY ACETABULAR CUP SYSTEM | JDI | 1997-03-21 | View |
| 510(k) | K963700 | METAGEN HIGH TIBIAL OSTEOTOMY SYSTEM | HRS | 1997-02-12 | View |
No matching devices.
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