FDA-Device2022-02-16Class II
ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
DePuy Orthopaedics, Inc.
Hazard
May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.
Sold states
US Nationwide distribution in the states of TN, TX.
Affected count
3 units
Manufactured in
700 Orthopaedic Dr, N/A, Warsaw, IN, United States
Products
ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0632-2022Don't want to check this manually?
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