Renovis Surgical Technologies, LLC
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K131354 | RENOVIS BIPOLAR HIP SYSTEM | KWY | 2013-09-19 | View |
| 510(k) | K131122 | S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM | OVD | 2013-09-18 | View |
| 510(k) | K120038 | A200 KNEE SYSTEM | OIY | 2013-02-14 | View |
| 510(k) | K112897 | RENOVIS SURGICAL HIP JOINT REPLACEMENT PROSTHESIS | OQG | 2012-06-13 | View |
| 510(k) | K111940 | S 100 PEDICLE SCREW SYSTEM | MNH | 2012-05-15 | View |
| 510(k) | K113084 | RENOVIS CANNULATED SCREW SYSTEM | HWC | 2011-12-09 | View |
| 510(k) | K110965 | RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM | KTT | 2011-05-11 | View |
| 510(k) | K101682 | S 100 PEDICLE SCREW SYSTEM | MNI | 2010-12-07 | View |
No matching devices.
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