510(k) K900927 ยท HQX Implant, Orbital, Extra-Ocular
CODERE-DURETTE ORBITAL FLOOR IMPLANT
| Applicant | Oculo Plastik, Inc., Montreal, Quebec Canada, CA |
| Decision | Substantially Equivalent, May 15, 1990 |
| Received | Feb 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900927
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.