Depuy Miltek, A Johnson & Johnson Co.
FDA 510(k) & PMA Approved Devices — 1 products
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Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K063273 | PANALOK QUICKANCHOR PLUS, PANALOK RC QUICKANCHOR PLUS DUAL SUTURE, PANALOK ANCHOR | JDR | 2006-11-22 | View |
No matching devices.
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