ClearanceBrief
510(k) K253676 · MRW System, Facet Screw Spinal Device

CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)

ApplicantProvidence Medical Technology, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, May 14, 2026
ReceivedNov 21, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253676

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.