510(k) K200002 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Anterior Spine Truss System Stand Alone (ASTS-SA) Interbody Fusion Device

Applicant	4Web, Inc., Frisco TX, US
Decision	Substantially Equivalent, May 29, 2020
Received	Jan 2, 2020
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K200002

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.