510(k) K160568 ยท PEK Spinous Process Plate
Precision Spine Interspinous Plate System
| Applicant | Precision Spine, Inc., Pearl MS, US |
| Decision | Substantially Equivalent, May 4, 2016 |
| Received | Feb 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160568
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.