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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: K040261
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Stryker Reflex Hybrid Level Anterior Cervical Plate; Non Sterile; Manufactured by Stryker Spine SAS... 2 08/20/2009 Stryker Spine
Stryker Reflex Hybrid Variable Self-Tapping Screw. Non Sterile. Manufactured by Stryker Spine, SAS... 2 08/20/2009 Stryker Spine
Stryker Reflex Hybrid variable self-drilling screw. Non Sterile. Manufactured by Stryker Spine SAS... 2 08/20/2009 Stryker Spine
Reflex Hybrid 4.0 x 14 mm Variable, Self-Tapping Bone Screw (Non- sterile). Manufactured by Stryker... 3 11/20/2008 Stryker Spine
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