510(k) K112551 ยท NKB Thoracolumbosacral Pedicle Screw System
S4 SPINAL SYSTEM
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 21, 2011 |
| Received | Sep 1, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112551
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.