ClearanceBrief
510(k) K201367 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

FlareHawk TiHawk9 Interbody Fusion System

ApplicantIntegrity Implants, Inc., Palm Beach Gardens FL, US
DecisionSubstantially Equivalent, Sep 23, 2020
ReceivedMay 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K201367

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.