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 |