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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: K123767
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Product Description
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FDA Recall
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LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip Driver - Short ("Driver... 2 11/26/2013 Lanx, Inc.
Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07, Model No. 86300204 ... 2 01/14/2015 Biomet Spine, LLC
Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205. Timberline Anchored Later... 2 01/15/2015 Biomet Spine, LLC
Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline... 2 01/15/2015 Biomet Spine, LLC
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