FDA UDI In Commercial Distribution 🇺🇸 United States

CREO

DI: 00889095067453 · Model: 1120.1500 · GLOBUS MEDICAL, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CREO
Primary DI
00889095067453
Version / Model
1120.1500
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-06
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
081971e9-a034-4625-9cc1-f0b3ca5fb3be

Device Description

6.0mm Straight Rod, Titanium Alloy, 500mm Length

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
MNH Orthosis, spondylolisthesis spinal fixation
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

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

Identifiers

Type ID
Primary 00889095067453

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K124058 000

Device Sizes

Type Value Unit Text
Length 500 Millimeter
Outer Diameter 6 Millimeter