FDA-Device2020-12-30Class II
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Biomet, Inc.
Hazard
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
Sold states
Worldwide distribution - US Nationwide distribution in the state of FL and the countries of Korea, Japan, Netherlands.
Affected count
21 units
Manufactured in
56 E Bell Dr, N/A, Warsaw, IN, United States
Products
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0723-2021Don't want to check this manually?
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