510(k) K132122 ยท KWP Appliance, Fixation, Spinal Interlaminal
KESTREL POSTERIOR CERVICAL SPINE SYSTEM
| Applicant | Omni Surgical, LLC Dba Spine360, Austin TX, US |
| Decision | Substantially Equivalent, Jan 22, 2014 |
| Received | Jul 10, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132122
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.