ClearanceBrief
510(k) K181980 ยท NKB Thoracolumbosacral Pedicle Screw System

OsseoScrew System

ApplicantAlphatec Spine, Inc., Carlsnad CA, US
DecisionSubstantially Equivalent, Sep 25, 2018
ReceivedJul 25, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181980

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.