510(k) K110367 ยท KWP Appliance, Fixation, Spinal Interlaminal
PIONEER SPINAL PROCESS FUSION PLATE
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Mar 23, 2011 |
| Received | Feb 8, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110367
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.