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 |