ClearanceBrief
510(k) K201605 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium ALIF Cage, EIT Cellular Titanium TLIF Cage, EIT Cellular Titanium LLIF Cage, EIT Cellular Titanium T/PLIF Cage

ApplicantEit Emerging Implant Technologies GmbH, Wurmlingen, DE
DecisionSubstantially Equivalent, Jul 15, 2020
ReceivedJun 15, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201605

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.