Orthopaedic Designs, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K971993 | ODI COMPRESSION HIP SCREW SYSTEM | KTT | 1997-11-12 | View |
| 510(k) | K880737 | SELF GUIDING (SG) INTERLOCKING NAIL | HSB | 1988-03-14 | View |
No matching devices.
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