510(k) K180156 · PEK Spinous Process Plate
SP-Fix® Spinous Process Fixation Plate, RELIEVE® Laminoplasty Fixation System
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Mar 7, 2018 |
| Received | Jan 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180156
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.