ClearanceBrief
510(k) K153386 ยท NKG Posterior Cervical Screw System

Perla Posterior Cervico-Thoracic Fixation system

ApplicantSpineart, Geneva, CH
DecisionSubstantially Equivalent, Jan 25, 2016
ReceivedNov 23, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K153386

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.