ClearanceBrief
510(k) K923616 ยท JDK Prosthesis, Hip, Cement Restrictor

OMNIFLEX-C UHMWPE MID-SHAFT RESTRICTOR

ApplicantOsteonics Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Oct 30, 1992
ReceivedJul 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923616

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.