FDA Device Intelligence
Home › ALPHATEC SPINE, INC. › IdentiTi II

IdentiTi II

ALPHATEC SPINE, INC. · Model 823-210 · UDI-DI 00190376595641

HXG Prescription
1
510(k) clearances
161
Adverse events (7 deaths)
0
Recalls
234
Facilities

Description

ID II TLIF-A, FOOTED TAMP

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.