510(k) K092295 ยท KWP Appliance, Fixation, Spinal Interlaminal
PIONEER POSTERIOR CERVICO-THORACIC SYSTEM
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Feb 19, 2010 |
| Received | Jul 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092295
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.