ClearanceBrief
510(k) K143488 ยท FMF Syringe, Piston

InFill Graft Delivery System

ApplicantPinnacle Spine Group, LLC, Dallas TX, US
DecisionSubstantially Equivalent, Dec 17, 2014
ReceivedDec 8, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K143488

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.