FDA UDI In Commercial Distribution 🇺🇸 United States

AERIAL

DI: 00889095717037 · Model: 1117.0231 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AERIAL
Primary DI
00889095717037
Version / Model
1117.0231
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-27
Public Version
1
Public Version Date
2019-07-05
Public Version Status
New
Public Device Record Key
376c62a1-ee04-489b-a450-31456edca09b

Device Description

AERIAL Implant 12x22mm, 9-15mm, 15°

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
PEK Spinous process plate

GMDN Terms

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

Identifiers

Type ID
Primary 00889095717037

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180817 000

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Height 9 Millimeter
Device Size Text, specify Lordosis 15 Degree
Width 12 Millimeter