Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K092815 |
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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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BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all in... | 2 | 07/05/2013 | SpineFrontier, Inc. |
S-LIFT Extension Shims Extension shims are manufactured from grade 5 titanium and are curved, recta... | 2 | 11/14/2013 | SpineFrontier, Inc. |
S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instrument to ad... | 2 | 07/05/2013 | SpineFrontier, Inc. |
S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: 11-50223 Product Usage: S... | 2 | 11/21/2012 | SpineFrontier, Inc. |
SpineFrontier S-Lift Lock Shaft Inserter, an instrument used with S-LIFT Intervertebral Body Fusion ... | 2 | 05/07/2014 | SpineFrontier, Inc. |
T-Handle, Strike Plate, Push Connection, Part Number: SI50023 Rev A T-handles are silicone handle... | 2 | 08/08/2013 | SpineFrontier, Inc. |
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