The following data is part of a premarket notification filed by Premia Spine Ltd. with the FDA for Versalink™ Fixation System.
Device ID | K182598 |
510k Number | K182598 |
Device Name: | VersaLink™ Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Premia Spine Ltd. 8 Hampton Ct Westfield, NJ 07090 |
Contact | Ron Sacher |
Correspondent | Janice Hogan Hogan Lovells 555 Thirteenth Street, Northwest Washington, DC 20004 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-20 |
Decision Date | 2018-11-13 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VERSALINK 86695601 5233175 Live/Registered |
XEROX CORPORATION 2015-07-16 |
VERSALINK 85852430 4851595 Live/Registered |
US LED Ltd. 2013-02-18 |
VERSALINK 78230883 2900757 Dead/Cancelled |
Datacom Systems, Inc. 2003-03-27 |
VERSALINK 77854862 3998851 Live/Registered |
Triton Systems of Delaware, LLC 2009-10-22 |
VERSALINK 76607226 3252144 Dead/Cancelled |
NETGEAR, INC. 2004-08-12 |
VERSALINK 76607226 3252144 Dead/Cancelled |
NETGEAR HOLDINGS LIMITED 2004-08-12 |
VERSALINK 76279711 not registered Dead/Abandoned |
Jethro, Inc. 2001-07-03 |
VERSALINK 76279708 not registered Dead/Abandoned |
Jethro, Inc. 2001-07-03 |
VERSALINK 76061695 not registered Dead/Abandoned |
Osteotech, Inc. 2000-06-02 |
VERSALINK 74516619 1937916 Live/Registered |
EVONIK DEGUSSA GMBH 1994-04-25 |