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VEO® Lateral Interbody Fusion System
Choice Spine, LP · Model 20-3006 · UDI-DI 00840996133012
HXG
Prescription
1
510(k) clearances
161
Adverse events (7 deaths)
0
Recalls
234
Facilities
Description
LATERAL,SPACER TAMP
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.