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IDENTITI

ALPHATEC SPINE, INC. · Model 100-08224500-S · UDI-DI 00190376205083

PHM MAX OVD Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

IDENTITi LIF POROUS Ti SPACER, 8 x 22 x 45 mm, 0°

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.