Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K040076 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ANSPACH***REF 98-0003***Sagittal microSaw Attachment Custom***Rx Only*** This device is intended ... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
ANSPACH***REF 98-0008***7cm Medium Attachment Custom***Rx Only*** This device is intended to be u... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
ANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used ... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
-