ClearanceBrief
510(k) K883783 ยท KWP Appliance, Fixation, Spinal Interlaminal

TSRH SACRAL SPINAL SCREW

ApplicantWarsaw Orthopedic, Inc., Warsaw IN, US
DecisionSubstantially Equivalent for Some Indications, Apr 6, 1989
ReceivedSep 6, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883783

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.