The following data is part of a premarket notification filed by Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular with the FDA for Axium Prime Detachable Coil System.
Device ID | K162704 |
510k Number | K162704 |
Device Name: | Axium Prime Detachable Coil System |
Classification | Device, Neurovascular Embolization |
Applicant | Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular 9775 Toledo Way Irvine, CA 92618 |
Contact | Joyce Zhong |
Correspondent | Joyce Zhong Micro Therapeutics, Inc. D/b/a Ev3 Neurovascular 9775 Toledo Way Irvine, CA 92618 |
Product Code | HCG |
CFR Regulation Number | 882.5950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-09-28 |
Decision Date | 2017-01-03 |
Summary: | summary |