ClearanceBrief
510(k) K201338 ยท FMF Syringe, Piston

Allograft MIS Delivery System

ApplicantLifenet Health, Virginia Beach VA, US
DecisionSubstantially Equivalent, Jul 13, 2020
ReceivedMay 20, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K201338

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.