510(k) K091782 ยท NKB Thoracolumbosacral Pedicle Screw System
REVERE 6.35 STABILIZATION SYSTEM
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Aug 13, 2009 |
| Received | Jun 17, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091782
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.