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Anterior Cervical Interbody Fusion Device

PRECISION SPINE, INC. · Model 02-9002 · UDI-DI 00840019916349

HXG Prescription
1
510(k) clearances
161
Adverse events (7 deaths)
0
Recalls
235
Facilities

Description

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Data 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.