ClearanceBrief
510(k) K965145 ยท KWP Appliance, Fixation, Spinal Interlaminal

DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

ApplicantDepuy, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Mar 13, 1997
ReceivedDec 23, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965145

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.