ClearanceBrief
510(k) K073515 ยท MRW System, Facet Screw Spinal Device

TRANS1 FACET SCREW

ApplicantTrans1 Incorporated, Wilmington NC, US
DecisionSubstantially Equivalent, Mar 11, 2008
ReceivedDec 14, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073515

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.