VersaLink™ Fixation System

Thoracolumbosacral Pedicle Screw System

Premia Spine Ltd.

The following data is part of a premarket notification filed by Premia Spine Ltd. with the FDA for Versalink™ Fixation System.

Pre-market Notification Details

Device IDK182598
510k NumberK182598
Device Name:VersaLink™ Fixation System
ClassificationThoracolumbosacral Pedicle Screw System
Applicant Premia Spine Ltd. 8 Hampton Ct Westfield,  NJ  07090
ContactRon Sacher
CorrespondentJanice Hogan
Hogan Lovells 555 Thirteenth Street, Northwest Washington,  DC  20004
Product CodeNKB  
CFR Regulation Number888.3070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-09-20
Decision Date2018-11-13
Summary:summary

NIH GUDID Devices

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Trademark Results [VersaLink]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERSALINK
VERSALINK
86695601 5233175 Live/Registered
XEROX CORPORATION
2015-07-16
VERSALINK
VERSALINK
85852430 4851595 Live/Registered
US LED Ltd.
2013-02-18
VERSALINK
VERSALINK
78230883 2900757 Dead/Cancelled
Datacom Systems, Inc.
2003-03-27
VERSALINK
VERSALINK
77854862 3998851 Live/Registered
Triton Systems of Delaware, LLC
2009-10-22
VERSALINK
VERSALINK
76607226 3252144 Dead/Cancelled
NETGEAR, INC.
2004-08-12
VERSALINK
VERSALINK
76607226 3252144 Dead/Cancelled
NETGEAR HOLDINGS LIMITED
2004-08-12
VERSALINK
VERSALINK
76279711 not registered Dead/Abandoned
Jethro, Inc.
2001-07-03
VERSALINK
VERSALINK
76279708 not registered Dead/Abandoned
Jethro, Inc.
2001-07-03
VERSALINK
VERSALINK
76061695 not registered Dead/Abandoned
Osteotech, Inc.
2000-06-02
VERSALINK
VERSALINK
74516619 1937916 Live/Registered
EVONIK DEGUSSA GMBH
1994-04-25

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