ClearanceBrief
510(k) K953076 ยท MRW System, Facet Screw Spinal Device

TOWNLEY FACET/PEDICULAR SCREW PLATING SYSTEM

ApplicantSofamor Danek USA,Inc., Memphis TN, US
DecisionSubstantially Equivalent, Feb 28, 1997
ReceivedJun 30, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953076

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.