FDA Device Intelligence
Home › Medacta International SA › Knee Instruments

Knee Instruments

Medacta International SA · Model 02.18.10.1270 · UDI-DI 07630971254084

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

Description

Tibia template size 1-2 Lateral

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.