The following data is part of a premarket notification filed by Blockade Medical, Llc (d.b.a. Balt Usa) with the FDA for Optima Coil System.
Device ID | K172390 |
510k Number | K172390 |
Device Name: | Optima Coil System |
Classification | Device, Neurovascular Embolization |
Applicant | Blockade Medical, LLC (d.b.a. Balt USA) 18 Technology Dr. Ste 169 Irvine, CA 92618 |
Contact | Rebecca K. Pine |
Correspondent | Rebecca K. Pine Blockade Medical, LLC (d.b.a. Balt USA) 18 Technology Dr. Ste 169 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 | 2017-08-08 |
Decision Date | 2018-02-18 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OPTIMA COIL SYSTEM 87266088 5586890 Live/Registered |
Blockade Medical LLC, a Balt Company 2016-12-12 |