ClearanceBrief
510(k) K051856 ยท MRW System, Facet Screw Spinal Device

TRANS1 FACET SCREWS

ApplicantTrans1 Incorporated, Wilmington NC, US
DecisionSubstantially Equivalent, Sep 26, 2005
ReceivedJul 8, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051856

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.