Synthes USA
411 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| BONE STAPLE(S) (K904553) | Synthes (Usa) | 1990-12-21 |
| SYNTHES EXTERNAL FIXATION BONE CLIP (K894098) | Synthes (Usa) | 1990-04-30 |
| MODULAR SPINAL FIXATION & LOCKING HOOK SPINAL ROD (K884688) | Synthes (Usa) | 1989-02-24 |
| CONDYLAR PROSTHESIS OF MANDIBLE W/HEAD (K840955) | Synthes (Usa) | 1984-06-19 |
| DYNAMIC CONDYLAR SCREW OR D.C.S. (K840954) | Synthes (Usa) | 1984-05-11 |
| MOBILIMB-CPM UPPER/LOWER LIMB DEVICE (K823495) | Synthes (Usa) | 1983-01-21 |
| SYNTHES SPINAL IMPLANT SYSTEM (K802462) | Synthes (Usa) | 1980-12-16 |
| SYNTHES RECONSTRUCTIVE PLATES 'Y' PLATES (K792291) | Synthes (Usa) | 1979-12-06 |
| ARICULATED TENSION DEVICE SYNTHES TEN (K792253) | Synthes (Usa) | 1979-12-05 |
| DYNAMIC HIP SCREW (K791619) | Synthes (Usa) | 1979-08-28 |
| OVERLOAD WARNING DEVICE (K770405) | Synthes (Usa) | 1977-03-10 |
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Every clearance here is in the API, with alerts when new ones post.