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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

DateFirmReason
2013-10-11Codman & Shurtleff, Inc.Incorrect instructions for use (IFU).
2013-10-11Codman & Shurtleff, Inc.Incorrect instructions for use (IFU).

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