Synthes (Usa), LLC
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K180821 | TruMatch Graft Cage - Long Bone | HRS | 2018-12-21 | View |
| 510(k) | K161417 | DePuy Synthes MAXFRAME Multi-Axial Correction System | KTT | 2016-11-10 | View |
| 510(k) | K130146 | SYNTHES SYNFLATE VERTEVRAL BALLOON SYSTEM | NDN | 2013-05-20 | View |
| 510(k) | K112030 | SYNTHES RADIAL HEAD PROSTHESIS SYSTEM | KWI | 2012-06-19 | View |
| 510(k) | K120275 | SYNTHES ACIS/VERTEBRAL SPACER CR | ODP | 2012-05-25 | View |
| 510(k) | K101536 | 2.7/3.5MM VA-LCP ANTERIRO CLAVICLE PLATE SYSTEM | HRS | 2010-09-15 | View |
No matching devices.
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