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Knee Instruments

Medacta International SA · Model 02.07.10.4082 · UDI-DI 07630040760454

LXH
10
510(k) clearances
81,662
Adverse events (55 deaths)
0
Recalls
1,115
Facilities

Description

Revision Trial extension stem Ø 20-65

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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.