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Solar™ Interbody Fusion System

DEGEN MEDICAL, INC. · Model 1203-382811L05 · UDI-DI 00842048167785

OVD MAX PHM Prescription

510(k) clearances

1,270

Adverse events (11 deaths)

Recalls

259

Facilities

Description

38W X 28D X 11H X 5° Solar™ Monolithic ALIF Spacer

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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.