ClearanceBrief
510(k) K934321 ยท HWC Screw, Fixation, Bone

LINVATEC STASYS-PES FIXATION DEVICE

ApplicantLinvatec Corp., Largo FL, US
DecisionSubstantially Equivalent, May 10, 1995
ReceivedSep 3, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934321

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.