Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K123164 |
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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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SpineFrontier MISquito Percutaneous Pedicle Screw System Surgical Technique; Part Number: DOC80023... | 2 | 04/21/2015 | SpineFrontier, Inc. |
PedFuse Bone Probe; Part: SI81008 spinal pedicle fixation. | 2 | 01/03/2014 | SpineFrontier, Inc. |
PedFuse Reset Screw Inserters; PedFuse Screw Inserter 05-7 REset Part #11-80110 The PedFuse Screw... | 2 | 12/20/2013 | SpineFrontier, Inc. |
PedFuse Reset Screw Inserters; PedFuse Screw Inserter 05-7 REspond Part# 11-80111 The PedFuse Scr... | 2 | 12/20/2013 | SpineFrontier, Inc. |
PedFuse Reset Screw Inserters; PedFuse Screw Inserter 08-9 REset Part# 11-80113 The PedFuse Screw... | 2 | 12/20/2013 | SpineFrontier, Inc. |
PedFuse Reset Screw; Model: 01-80115-55 The PedFuse Reset pedicle screw implants intended to be u... | 2 | 12/19/2013 | SpineFrontier, Inc. |
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