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MEDTRONIC SOFAMOR DANEK, INC. · Model 8114502 · UDI-DI 00613994158291

LXH
10
510(k) clearances
81,662
Adverse events (55 deaths)
0
Recalls
1,117
Facilities

Description

INSTRUMENT 8114502 MSRNG CALPR 4.5MM RD

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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.