510(k) K111183 ยท KWP Appliance, Fixation, Spinal Interlaminal
ASCENT POSTERIOR OCCIPITAL THORACIC (POCT) SYSTEM (TITANIUM & COBALT CHROME RODS)
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, May 24, 2011 |
| Received | Apr 27, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111183
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.