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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K153452
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FDA Recall
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Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Left, Product No. LJV193T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T 2 04/16/2019 Integra LifeSciences Corp.
Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T 2 04/16/2019 Integra LifeSciences Corp.
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