FDA Device Intelligence
Home › ALPHATEC SPINE, INC. › Calibrate

Calibrate

ALPHATEC SPINE, INC. · Model 261-06184515-D · UDI-DI 00190376522654

PHMOVDMAX Prescription
1
510(k) clearances
23
Adverse events
0
Recalls
84
Facilities

Description

LTX DOMED SPACER, 6 x 18 x 45 mm, 15°

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.