Medical Device Recalls
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1 to 10 of 23 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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|---|---|---|---|
| 90 DEG RIGHT ANGLE ATTACH, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| 45 degree Contra Angle Attachment Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| 6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| B-SAGITTAL ASSEMBLY Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| GREEN ROTATING CRANIOTOME, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| ADJUSTABLE DRILL GUIDE, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| 16CM MIN INVASIVE ATTACH, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| 22CM MICRO REVISION ATTACH, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
| 16.5CM MICRO REVISION ATTACH, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
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