Cohort Medical Products Group, Inc.
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) | K964975 | COHORT DISCECTOMY SYSTEMS (CDS) | HRX | 1997-02-24 | View |
| 510(k) | K950011 | COHORT(TM) ANTERIOR PLATE SYSTEM (APS) | KWQ | 1995-11-06 | View |
| 510(k) | K943804 | BONE SCREW | HWC | 1994-12-08 | View |
| 510(k) | K943472 | COHORT AVB RETRACTOR SYSTEM | HXB | 1994-10-20 | View |
| 510(k) | K943474 | CANNULATED BONE SCREW | HWC | 1994-10-14 | View |
No matching devices.
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