The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Quartex™ Occipito-cervico-thoracic Spinal System, Globus Navigation Instruments.
Device ID | K161591 |
510k Number | K161591 |
Device Name: | QUARTEX™ Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments |
Classification | Posterior Cervical Screw System |
Applicant | GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
Contact | Kelly J. Baker |
Correspondent | Kelly J. Baker, Ph.d. GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 |
Product Code | NKG |
Subsequent Product Code | KWP |
Subsequent Product Code | OLO |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-09 |
Decision Date | 2016-09-21 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUARTEX 87678551 5502026 Live/Registered |
Adam Matthew Digital Limited 2017-11-09 |
QUARTEX 87476750 5369701 Live/Registered |
Primex, Inc. 2017-06-06 |
QUARTEX 86924329 5152648 Live/Registered |
Globus Medical Inc. 2016-03-01 |
QUARTEX 78827280 not registered Dead/Abandoned |
International Watch Group, Inc. 2006-03-02 |
QUARTEX 74075808 1814537 Dead/Cancelled |
QUARTEX CORPORATION, THE 1990-07-06 |
QUARTEX 73526499 1365875 Dead/Cancelled |
KAWASHO INTERNATIONAL (U.S.A.) INC. 1985-03-12 |
QUARTEX 73461448 1326845 Dead/Cancelled |
Eastern Watch Co., Inc. 1984-01-16 |
QUARTEX 73346115 not registered Dead/Abandoned |
DELTA IMPEX WATCH CORP. 1982-01-18 |
QUARTEX 73335177 not registered Dead/Abandoned |
QUARTEX, INC. 1981-11-02 |
QUARTEX 72316823 0881565 Dead/Expired |
RANCO INDUSTRIAL PRODUCTS CORPORATION 1969-01-16 |