ClearanceBrief
510(k) K170821 · NKB Thoracolumbosacral Pedicle Screw System

ChoiceSpine™ Proliant® Posterior Pedicle Screw and Hook Fixation System

ApplicantChoicespine, LP, Knoxville TN, US
DecisionSubstantially Equivalent, Jun 8, 2017
ReceivedMar 20, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170821

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.