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Solar™ Interbody Fusion System

DEGEN MEDICAL, INC. · Model 1203-382611L10 · UDI-DI 00842048166344

PHM OVD MAX Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

38W X 26D X 11H X 10° 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.