510(k) K122310 ยท HRS Plate, Fixation, Bone
GEMINUS FOSSA SPECIFIC PLATE SYSTEM
| Applicant | Skeletal Dynamics, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Jan 18, 2013 |
| Received | Aug 1, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122310
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.