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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 31 Results
510(K) Number: K073437
 
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Product Description
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Recall
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FDA Recall
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Stryker Thor Anterior Plating System; Non Sterile Thor Standard Screw 6.0 x 25MM, spinal implant c... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.5 x 67MM, spinal imp... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Screw 6.0 x 31MM, spinal implant c... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Screw 6.0 x 34MM, spinal implant c... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Screw 6.0 x 37MM, spinal implant c... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 40MM, spinal imp... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 43MM, spinal imp... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 46MM, spinal imp... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 49MM, spinal imp... 2 11/24/2009 Stryker Spine
Stryker Thor Anterior Plating System; Non Sterile Thor Standard Long Screw 6.0 x 52MM, spinal imp... 2 11/24/2009 Stryker Spine
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