510(k) K050979 ยท MNI Orthosis, Spinal Pedicle Fixation
S4 SPINAL SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 27, 2005 |
| Received | Apr 19, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050979
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.