510(k) K162211 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
AccuFit Lateral Plate System
| Applicant | Precision Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Nov 28, 2016 |
| Received | Aug 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162211
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.