ClearanceBrief
510(k) K213653 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

4CIS BLACK MARLIN PLIF CAGE SYSTEM, 4CIS DOLPHIN TLIF CAGE SYSTEM

ApplicantSolco Biomedical Company India Private Limited, Ahmedabad, IN
DecisionSubstantially Equivalent, Dec 19, 2022
ReceivedNov 19, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213653

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.