510(k) K072081 ยท KWP Appliance, Fixation, Spinal Interlaminal
ZODIAC DYNAMO SEMI-RIGID SPINAL SYSTEM
| Applicant | Alphatec Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Oct 24, 2007 |
| Received | Jul 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072081
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.