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

Ascend

ALPHATEC SPINE, INC. · Model 153-12-L-164505-S · UDI-DI 00190376519081

PLR Prescription
1
510(k) clearances
13
Adverse events
0
Recalls
70
Facilities

Description

12 mm CORE ENDPLATE, LAT 16 x 45 mm 5°

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.