FDA Device Intelligence
HomeMedacta International SA › Hip Instruments

Hip Instruments

Medacta International SA · Model 01.15.10.0168 · UDI-DI 07630040735599

FWX
3
510(k) clearances
17
Adverse events
1
Recalls
14
Facilities

Description

Black Thigh elevator

Recalls

DateFirmReason
2008-05-21Medacta Usa IncMedacta is issuing this Recall because improper connection of the table clamping mechanism may result in the AMIS table becoming separated from the surgical table resulting in inju

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.