Medical Device Recalls
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11 to 20 of 23 Results
510(K) Number: K955084 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
10.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
14CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
13.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
8CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
7.5CM ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
B-SAGITTAL ASSEMBLY 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. |
45 degree Contra Angle Attachment Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
16CM MIN INVASIVE ATTACH, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
ADJUSTABLE DRILL GUIDE, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
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