Medical Device Recalls
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21 to 23 of 23 Results
510(K) Number: K955084 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
GREEN ROTATING CRANIOTOME, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system | 2 | 05/04/2017 | The Anspach Effort, Inc. |
CONTRA ANGLE ATTACHMENT, BLACK MAX | 2 | 05/04/2017 | The Anspach Effort, Inc. |
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