510(k) K090222 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PIONEER LUMBAR PLATE SYSTEM
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Apr 28, 2009 |
| Received | Jan 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090222
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.