ClearanceBrief
510(k) K192354 ยท NKG Posterior Cervical Screw System

Innovasis Gibralt Spine System

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Sep 24, 2019
ReceivedAug 29, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K192354

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.