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 |