ClearanceBrief
510(k) K071334 ยท HAW Neurological Stereotaxic Instrument

DEPUY CAS HEMI ASR HIP INSTRUMENTS

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 2, 2007
ReceivedMay 11, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071334

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.