ClearanceBrief
510(k) K253432 · MRW System, Facet Screw Spinal Device

DiversiVy™ Facet Screw System

ApplicantVy Spine, LLC, Bountiful UT, US
DecisionSubstantially Equivalent, Mar 19, 2026
ReceivedOct 1, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253432

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.