510(k) K150851 ยท KWP Appliance, Fixation, Spinal Interlaminal
Sure Lok Mini Posterior Cervical/Upper Thoracic System
| Applicant | Precision Spine, Inc., Pear MS, US |
| Decision | Substantially Equivalent, Jun 4, 2015 |
| Received | Mar 31, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150851
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.