ClearanceBrief
510(k) K231456 · FMF Syringe, Piston

Avitus® DragonWing Large Volume Autograft Delivery System

ApplicantAvitus Orthopaedics, Inc., Shelton CT, US
DecisionSubstantially Equivalent, Jul 17, 2023
ReceivedMay 19, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231456

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.