ClearanceBrief
510(k) K161499 ยท NKB Thoracolumbosacral Pedicle Screw System

VertiForm Posterior Fixation System

ApplicantNext Orthosurgical, Vista CA, US
DecisionSubstantially Equivalent, Jul 29, 2016
ReceivedJun 1, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K161499

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.