Shoulder Options, 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) | K121672 | AFT PROXIMAL HUMERUS FRACTURE PLATE | HRS | 2012-10-01 | View |
| 510(k) | K102539 | ICUFF REPAIR PLATE, RIGHT; CUFF REPAIR PLATE. LEFT; ANCHOR BOLT, 10MM THROUGH 50MM | MBI | 2011-02-24 | View |
No matching devices.
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