FDA-Device2013-11-06Class II
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Zimmer, Inc.
Hazard
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Sold states
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Dominican Republic, Ecuador, El Salvador, Germany, Guatemala, Honduras, Hong Kong, India, Israel, Jamaica, Japan, Korea, Malaysia, Mexico, New Zealand, Nicaragua, Panama, Peru, Singapore, Taiwan, Thailand, and Venezula.
Affected count
32537
Manufactured in
345 E Main St, N/A, Warsaw, IN, United States
Products
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0076-2014Don't want to check this manually?
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