FDA Device Intelligence
HomeDEPUY SPINE, LLC › NA

NA

DEPUY SPINE, LLC · Model 698342610 · UDI-DI 10705034491004

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

Description

MODIFIED INSTRUMENT TAMP 5X15mm

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.