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 |