FDA Device Intelligence
Home › ALPHATEC SPINE, INC. › Intervertebral Disc Preparation Instruments

Intervertebral Disc Preparation Instruments

ALPHATEC SPINE, INC. · Model 256-01-300-11 · UDI-DI 00190376378657

GFI Prescription
6
510(k) clearances
61
Adverse events
0
Recalls
145
Facilities

Description

LIF, OSTEOTOME, MEDIAL UP, 11MM

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.