Vertelink Corporation
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) | K032102 | VERTELINK KOBRA SPINAL FIXATION SYSTEM | KWQ | 2003-12-12 | View |
| 510(k) | K030734 | PATHWAY ACCESS SHEATH CATHETER | DYB | 2003-09-10 | View |
| 510(k) | K030662 | PATHWAY ACCESS SHEATH CATHETER | EZN | 2003-09-03 | View |
No matching devices.
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