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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K051976
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Product Description
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Recall
Class
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FDA Recall
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StelKast Proven Knee System - Tibial Half Block Augmentation and Screw. Part Number SC2287-1-5, Siz... 3 01/23/2008 FEI # 3004142400
Stelkast Co
StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number SC2287-2-5, Size 2 Thi... 3 01/23/2008 FEI # 3004142400
Stelkast Co
StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number: SC2287-5-5, Size 5, ... 3 01/23/2008 FEI # 3004142400
Stelkast Co
StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number SC2287-4-5, Size 4, Th... 3 01/23/2008 FEI # 3004142400
Stelkast Co
StelKast Proven Knee - Tibial Half Block Augmentation and Screw. Part Number SC2287-3-5, Size 3, Th... 3 01/23/2008 FEI # 3004142400
Stelkast Co
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