Home › Device types › KGG
Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations
FDA product code KGG · Class 3 · Unknown
4
Registered devices
98
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-10-11 | Codman & Shurtleff, Inc. | Incorrect instructions for use (IFU). |
| 2013-10-11 | Codman & Shurtleff, Inc. | Incorrect instructions for use (IFU). |
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