FDA Device Intelligence
HomeMEDTRONIC SOFAMOR DANEK, INC. › N/A

N/A

MEDTRONIC SOFAMOR DANEK, INC. · Model 945DAQ916 · UDI-DI 00643169071933

GWSGWEGWJGWFGWQ
1
510(k) clearances
2
Adverse events
0
Recalls
10
Facilities

Description

AMPLIFIER 945DAQ916 DIG PREAMPLIFIER

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.