ClearanceBrief
510(k) K936294 ยท KWP Appliance, Fixation, Spinal Interlaminal

SENTRY(TM) ANTERIOR/POSTERIOR SPINAL SYSTEMS

ApplicantSofamor Danek Mfg., Inc., Memphis TN, US
DecisionSubstantially Equivalent for Some Indications, Dec 19, 1995
ReceivedDec 10, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936294

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.