The following data is part of a premarket notification filed by Micro Therapeutics, Inc. with the FDA for Axium Detachable Coil System.
| Device ID | K081465 |
| 510k Number | K081465 |
| Device Name: | AXIUM DETACHABLE COIL SYSTEM |
| Classification | Device, Vascular, For Promoting Embolization |
| Applicant | MICRO THERAPEUTICS, INC. 9775 TOLEDO WAY Irvine, CA 92618 |
| Contact | Neelu Medhekar |
| Correspondent | Neelu Medhekar MICRO THERAPEUTICS, INC. 9775 TOLEDO WAY Irvine, CA 92618 |
| Product Code | KRD |
| CFR Regulation Number | 870.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-05-27 |
| Decision Date | 2008-08-19 |
| Summary: | summary |