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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K051918
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Product Description
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Recall
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FDA Recall
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Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ O... 2 03/11/2019 FEI # 1000519909
Ossur Americas
Ossur, J Tong, Sterile, Part/ Description: JT-115/ J TONG MED/LGE-No App; JT-200/ J TONG ASSEM... 2 03/11/2019 FEI # 1000519909
Ossur Americas
Ossur, Sterile, Part/ Description: 505300T/ CB RING KIT TI SM; 505300V2/ OB V2 RING KIT TI SM;... 2 03/11/2019 FEI # 1000519909
Ossur Americas
Ossur CB Resolve, Sterile, Part/ Description: 505300C/ CB RESOLVE STERILE UNIT SML; 505400C/ C... 2 03/11/2019 FEI # 1000519909
Ossur Americas
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