510(k) K241438 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Signus Tetris St; Signus Tetris R St

Applicant	Signus Medizintechnik GmbH, Alzenau, DE
Decision	Substantially Equivalent, Sep 11, 2024
Received	May 21, 2024
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K241438

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.