ClearanceBrief
510(k) K964882 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

IMPLEX REPLACEMENT ACETABULAR CUP INSERT

ApplicantImplex Corp., Allendale NJ, US
DecisionSubstantially Equivalent, Mar 13, 1997
ReceivedDec 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964882

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.