510(k) K181644 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar

EIT Cellular Titanium® Lumbar Cage LLIF

Applicant	Eit Emerging Implant Technologies GmbH, Wurmlingen, DE
Decision	Substantially Equivalent, Oct 12, 2018
Received	Jun 22, 2018
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K181644

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.