510(k) K120724 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
PIONEER LATERAL PLATE SYSTEM
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, May 7, 2012 |
| Received | Mar 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120724
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.