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IdentiTi

ALPHATEC SPINE, INC. · Model CI-10299-05141207 · UDI-DI 00811801033698

PHMMAXOVDODP Prescription
1
510(k) clearances
23
Adverse events
0
Recalls
82
Facilities

Description

CERVICAL TRIAL, 5 x 14 x 12 mm, 7° - FLUSH STOP

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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.