ClearanceBrief
510(k) K201481 ยท NKG Posterior Cervical Screw System

Centurion POCT System

ApplicantOrthofix, Inc., Lewisville TX, US
DecisionSubstantially Equivalent, Jun 15, 2020
ReceivedJun 4, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201481

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.