510(k) K073232 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXX
| Applicant | Spinefrontier, Inc., Beverly MA, US |
| Decision | Substantially Equivalent, Feb 20, 2008 |
| Received | Nov 15, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073232
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.