ClearanceBrief
510(k) K924323 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

THE UNIVERSAL BONE CEMENT RESISTOR

ApplicantBiodynamic Technologies, Inc., Arlington VA, US
DecisionSubstantially Equivalent, Feb 12, 1993
ReceivedAug 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924323

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.