Medical Device Recalls
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1 to 10 of 22 Results
510(K) Number: K955084 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| GREEN ROTATING CRANIOTOME, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems inclu... | 2 | 11/13/2013 |
FEI # 1045834 The Anspach Effort, Inc. |
| CONTRA ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| B-SAGITTAL ASSEMBLY Product Usage: Pneumatic system | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including th... | 2 | 07/03/2014 |
FEI # 1045834 The Anspach Effort, Inc. |
| ADJUSTABLE DRILL GUIDE, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 90 degree Contra Angle Attachment Product Usage: Pneumatic system | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 90 DEG RIGHT ANGLE ATTACH, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 9.4CM MICRO REVISION ATTACH, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
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