ClearanceBrief
510(k) K002959 ยท KWP Appliance, Fixation, Spinal Interlaminal

MODIFICATION TO ISOBAR SPINAL SYSTEM

ApplicantEncore Orthopedics, Inc., Austin TX, US
DecisionSubstantially Equivalent, Oct 16, 2000
ReceivedSep 22, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002959

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.