Medical Device Recalls
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11 to 20 of 22 Results
510(K) Number: K955084 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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. |
| 11CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 10.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 14CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 13.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 8CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 |
FEI # 1045834 The Anspach Effort, Inc. |
| 7.5CM ANGLE ATTACHMENT, BLACK MAX | 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. |
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