Integra Life Sciences
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120600 | DURAGEN SECURE DURAL REGNERATION MATRIX | GXQ | 2012-06-15 | View |
| 510(k) | K103248 | INTEGRITY SPINAL CARE SYSTEM | ITH | 2011-04-05 | View |
| 510(k) | K103742 | ACCELL EVO3 (FORMERLY ACCELL A2I) | MBP | 2011-03-17 | View |
No matching devices.
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