FDA UDI In Commercial Distribution 🇺🇸 United States

CREO

DI: 00889095014778 · Model: 1067.1176S · GLOBUS MEDICAL, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CREO
Primary DI
00889095014778
Version / Model
1067.1176S
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
569ceb13-bdc9-428c-ae35-4f2df88a729a

Device Description

CREO AMP 10.5 x 75mm HA Coated Modular Screw

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
MNI Orthosis, spinal pedicle fixation
MNH Orthosis, spondylolisthesis spinal fixation
KWQ Appliance, fixation, spinal intervertebral body
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 00889095014778

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K124058 000

Device Sizes

Type Value Unit Text
Length 75 Millimeter
Outer Diameter 10.5 Millimeter