ClearanceBrief
510(k) K043223 ยท HAW Neurological Stereotaxic Instrument

DEPUY CAS KNEE INSTRUMENTATION

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Mar 4, 2005
ReceivedNov 22, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043223

DateFirm and productCodeLinked 510(k)
Feb 13, 2020DePuy Orthopaedics, Inc.
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
Terminated
HTZNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.