Renovis Surgical Technologies
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Renovis A200 PS Knee System as part of the Renovis A200 Knee System (K190122) | Renovis Surgical Technologies | 2019-06-20 |
| Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System (K182007) | Renovis Surgical Technologies | 2018-12-07 |
| Renovis S180 Lateral Lumbar Interbody Fusion System (K181655) | Renovis Surgical Technologies | 2018-09-11 |
| Renovis Surgical Hip Replacement System (K171543) | Renovis Surgical Technologies | 2017-11-16 |
| Renovis S141 Lumbar Interbody Fusion System (K170888) | Renovis Surgical Technologies | 2017-08-08 |
| Renovis Tesera SC Stand-alone Anterior Cervical Fusion (ACF) System (K153250) | Renovis Surgical Technologies | 2016-03-16 |
| Renovis S141 Lumbar Interbody Cage System (K143126) | Renovis Surgical Technologies | 2015-02-06 |
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Every clearance here is in the API, with alerts when new ones post.