The following data is part of a premarket notification filed by Kinamed, Incorporated with the FDA for Supercable® Iso-elastic™ Cerclage System.
Device ID | K181749 |
510k Number | K181749 |
Device Name: | SuperCable® Iso-Elastic™ Cerclage System |
Classification | Cerclage, Fixation |
Applicant | Kinamed, Incorporated 820 Flynn Road Camarillo, CA 93010 |
Contact | Heather Neely |
Correspondent | Heather Neely Kinamed, Incorporated 820 Flynn Road Camarillo, CA 93010 |
Product Code | JDQ |
CFR Regulation Number | 888.3010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-07-02 |
Decision Date | 2018-08-01 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUPERCABLE 86020183 4673174 Live/Registered |
Engineering Seismology Group Canada Inc. 2013-07-25 |
SUPERCABLE 85153086 4069578 Live/Registered |
Kinamed, Inc. 2010-10-14 |
SUPERCABLE 78058674 not registered Dead/Abandoned |
AG Communication Systems Corporation 2001-04-16 |
SUPERCABLE 77279493 not registered Dead/Abandoned |
Supercable, S.A. 2007-09-14 |
SUPERCABLE 76193367 not registered Dead/Abandoned |
IGC-SuperPower, LLC 2001-01-11 |
SUPERCABLE 74696380 not registered Dead/Abandoned |
Blockbuster Entertainment Inc. 1995-06-29 |
SUPERCABLE 73778406 1605169 Dead/Cancelled |
MPC TECHNOLOGIES CO. 1989-02-02 |
SUPERCABLE 73437443 1312816 Dead/Cancelled |
American Bentley, Inc. 1983-08-01 |