Core Essence Orthopaedics, LLC
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) | K081060 | FERROFIBRE STAINLESS STEEL SUTURES, MODEL 610 SERIES SIZES (USP) 5-0 TO #5 | GAQ | 2008-12-24 | View |
| 510(k) | K071477 | REVERTO 55 AND 37 SHAPE MEMORY STAPLES | JDR | 2007-08-15 | View |
| 510(k) | K071520 | RENOVO SUTURE ANCHORS, MODELS 100-2001 THRU 100-5502X | MBI | 2007-08-10 | View |
No matching devices.
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