510(k) K181063 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Kestrel Buttress Plate System
| Applicant | Innovasis, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 13, 2018 |
| Received | Apr 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181063
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.