FDA UDI In Commercial Distribution 🇺🇸 United States

CREO

DI: 00889095209402 · Model: 7120.3050 · GLOBUS MEDICAL, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CREO
Primary DI
00889095209402
Version / Model
7120.3050
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c6d6452c-316d-4627-a819-9ebf557d5312

Device Description

6.0mm Curved Rod, Cobalt Chrome, 50mm 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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

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

Identifiers

Type ID
Primary 00889095209402

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K124058 000

Device Sizes

Type Value Unit Text
Outer Diameter 6 Millimeter
Length 50 Millimeter