The following data is part of a premarket notification filed by Codman & Shurtleff, Inc with the FDA for Codman Microcoil Delivery System, Deltamaxx Microcoil Delivery System, Orbit Galaxy G2 Microcoil Delivery System, Enpower Control Cable, Connector Cable.
Device ID | K142429 |
510k Number | K142429 |
Device Name: | CODMAN Microcoil Delivery System, DELTAMAXX Microcoil Delivery System, ORBIT GALAXY G2 Microcoil Delivery System, EnPower Control Cable, Connector Cable |
Classification | Device, Neurovascular Embolization |
Applicant | Codman & Shurtleff, Inc 325 Paramount Drive Raynham, MA 02767 |
Contact | Hannah Foley |
Correspondent | Hannah Foley Codman & Shurtleff, Inc 325 Paramount Drive Raynham, MA 02767 |
Product Code | HCG |
CFR Regulation Number | 882.5950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-29 |
Decision Date | 2014-12-24 |
Summary: | summary |