ClearanceBrief
510(k) K183589 ยท MRW System, Facet Screw Spinal Device

PMT Facet Screw

ApplicantProvidence Medical Technology, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Oct 11, 2019
ReceivedDec 21, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183589

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.