The following data is part of a premarket notification filed by Microvention, Inc. with the FDA for Microplex Coil System (mcs) And Hydrocoil Embolic System (hes).
Device ID | K050954 |
510k Number | K050954 |
Device Name: | MICROPLEX COIL SYSTEM (MCS) AND HYDROCOIL EMBOLIC SYSTEM (HES) |
Classification | Device, Neurovascular Embolization |
Applicant | MICROVENTION, INC. 75 COLUMBIA Aliso Viejo, CA 92656 -1408 |
Contact | Vincent Cutarelli |
Correspondent | Vincent Cutarelli MICROVENTION, INC. 75 COLUMBIA Aliso Viejo, CA 92656 -1408 |
Product Code | HCG |
CFR Regulation Number | 882.5950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-04-15 |
Decision Date | 2005-06-28 |
Summary: | summary |