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Solar™ Interbody Fusion System

DEGEN MEDICAL, INC. · Model 1203-422821L05 · UDI-DI 00842048169727

PHM OVD MAX Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

42W X 28D X 21H 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.