ClearanceBrief
510(k) K003928 ยท MRW System, Facet Screw Spinal Device

TOWNLEY TRANSFACETPEDICULAR SCREW FIXATION SYSTEM

ApplicantMedtronic Sofamor Danek, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Jan 17, 2001
ReceivedDec 20, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K003928

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.