ClearanceBrief
510(k) K092464 ยท MRW System, Facet Screw Spinal Device

SPINEOLOGY FACET SCREW

ApplicantSpineology, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Nov 9, 2009
ReceivedAug 11, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092464

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.