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U2 Total Knee System

UNITED ORTHOPEDIC CORP. · Model 9303-3207-RA · UDI-DI 04719886903386

LXH Prescription
10
510(k) clearances
82,132
Adverse events (55 deaths)
0
Recalls
1,119
Facilities

Description

Pin, Ø3.2mm×70mm

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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.