510(k) K150229 ยท KWP Appliance, Fixation, Spinal Interlaminal
SOLSTICE OCT System
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Apr 7, 2015 |
| Received | Feb 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150229
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.