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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: K080108
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Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979 2 07/20/2021 FEI # 3004024955
Stryker Spine
Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962 2 07/20/2021 FEI # 3004024955
Stryker Spine
Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010 2 05/05/2020 FEI # 3004024955
Howmedica Osteonics Corp.
Orthovita(R) Cortoss(TM) Delivery Gun Product Usage: Used for the application of Cortoss(TM) B... 2 09/12/2011 FEI # 1000307073
Orthovita, Inc.
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