510(k) K062327 ยท NKB Thoracolumbosacral Pedicle Screw System
MODIFICATION TO S4 SPINAL SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Mar 14, 2007 |
| Received | Aug 10, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062327
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.