ClearanceBrief
510(k) K982011 ยท KWP Appliance, Fixation, Spinal Interlaminal

DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Aug 6, 1998
ReceivedJun 8, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982011

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.