510(k) K060152 ยท MNI Orthosis, Spinal Pedicle Fixation
MODIFICATION TO S4 SPINAL SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Feb 3, 2006 |
| Received | Jan 20, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060152
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.