510(k) K122211 ยท HAW Neurological Stereotaxic Instrument
SYNTHES NAVIGABLE PEDICLE PREPARATION INSTRUMENTS
| Applicant | Synthes Spine, West Chester PA, US |
| Decision | Substantially Equivalent, Dec 17, 2012 |
| Received | Jul 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122211
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.