FDA UDI In Commercial Distribution 🇺🇸 United States

CREO

DI: 00889095791013 · Model: 5156.2275 · GLOBUS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CREO
Primary DI
00889095791013
Version / Model
5156.2275
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-29
Public Version
1
Public Version Date
2019-07-08
Public Version Status
New
Public Device Record Key
c06a51a9-41bf-4890-8457-fdeb27587bd0

Device Description

CREO DLX Polyaxial DOD Screw, 8.0-6.5x75mm

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

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

Identifiers

Type ID
Primary 00889095791013

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182375 000

Device Sizes

Type Value Unit Text
Outer Diameter 8 Millimeter
Outer Diameter 6.5 Millimeter
Length 75 Millimeter