510(k) K101682 ยท MNI Orthosis, Spinal Pedicle Fixation
S 100 PEDICLE SCREW SYSTEM
| Applicant | Renovis Surgical Technologies, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Dec 7, 2010 |
| Received | Jun 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101682
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.