Core Essence Orthopaedics, 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) | K101126 | PONTIS SUTURES AND SUTURE ANCHORS WITH OPTIONAL CRIMPS | MBI | 2010-12-02 | View |
| 510(k) | K090128 | TAC-TITE (TM) | GAT | 2009-03-19 | View |
No matching devices.
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