FDA UDI In Commercial Distribution 🇺🇸 United States

QUARTEX

DI: 00889095355666 · Model: 1149.4248 · GLOBUS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QUARTEX
Primary DI
00889095355666
Version / Model
1149.4248
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-15
Public Version
1
Public Version Date
2019-11-25
Public Version Status
New
Public Device Record Key
2653d65e-524b-4f44-8c13-4486a9cbb8a1

Device Description

QUARTEX 4.0mm Polyaxial Shoulder Screw, 48mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKG Posterior cervical screw system
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
37272 Trans-facet-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00889095355666

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161591 000

Device Sizes

Type Value Unit Text
Length 48 Millimeter
Outer Diameter 4 Millimeter