Food and Drug Administration

Neurological Devices Panel Meeting

August 5, 2003

Disclaimer

The statements contained in this document(s) are those of the product's sponsor, not FDA, and FDA does not necessarily agree with the sponsor's statements. FDA has not made a final determination about the safety or effectiveness of the product described in this document.

Onyx Liquid Embolic System (ES), Micro Therapeutics (HTM) (PPT)

Micro Therapeutics, Inc. Onyx® Liquid Embolic System (Onyx® LES), Dr. Peter Hudson, PhD, Dr. Ann Costello, PhD, DMD, Judy Chen, FDA (HTM) (PPT)