ClearanceBrief
510(k) K173522 · NKB Thoracolumbosacral Pedicle Screw System

Solanas® Posterior Stabilization System

ApplicantAlphatec Spine, Inc., Carlsnad CA, US
DecisionSubstantially Equivalent, Nov 30, 2017
ReceivedNov 14, 2017
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K173522

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.