ClearanceBrief
510(k) K172469 ยท NKB Thoracolumbosacral Pedicle Screw System

TiLock Modular Spinal System

ApplicantGenesys Spine, Austin TX, US
DecisionSubstantially Equivalent, Nov 30, 2017
ReceivedAug 15, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172469

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.