ClearanceBrief
510(k) K190071 · NKG Posterior Cervical Screw System

Perla® Posterior Cervico-Thoracic Fixation System

ApplicantSpineart, Plan Les Ouates, CH
DecisionSubstantially Equivalent, Feb 25, 2019
ReceivedJan 15, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K190071

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.