Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K060428 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CSS-059-70-5, Modified 7.0 mm Modified Depth Gauge, Lot 0985031 | 2 | 11/26/2010 | Orthohelix Surgical Designs Inc |
CSS-059-40-4 Modified 4.0mm Modified Depth Gauge, Lot 0985011 | 2 | 11/26/2010 | Orthohelix Surgical Designs Inc |
CSS-059-55-4, Modified 5.5 mm Modified Depth Gauge, Lot 0985021 | 2 | 11/26/2010 | Orthohelix Surgical Designs Inc |
MaxTorque Cannulated Screw Model # MSD-010-55-060S | 2 | 04/06/2010 | Orthohelix Surgical Designs Inc |
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