ClearanceBrief
510(k) K221182 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Southern Transforaminal Lumbar Interbody Fusion (TLIF)

ApplicantSouthern Medical (Pty) , Ltd., Irene, ZA
DecisionSubstantially Equivalent, Dec 8, 2022
ReceivedApr 25, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221182

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.