ClearanceBrief
510(k) K203327 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

VERTACONNECT TLIF Cage

ApplicantSignus Medizintechnik, Alzenau, DE
DecisionSubstantially Equivalent, Jan 25, 2021
ReceivedNov 12, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203327

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.