510(k) K121725 ยท KWP Appliance, Fixation, Spinal Interlaminal
PIONEER POSTERIOR OCCIPITO-CERVICO-THORACIC (OCT) SYSTEM
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Nov 7, 2012 |
| Received | Jun 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121725
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.