FDA UDI In Commercial Distribution 🇺🇸 United States

RESONATE

DI: 00193982154752 · Model: 1194.2024 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESONATE
Primary DI
00193982154752
Version / Model
1194.2024
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-28
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
6dca45be-45a9-48f5-8829-0e7fbf4f7382

Device Description

RESONATE Anterior Cervical Plate, 2-Level, 24mm

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
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00193982154752

Premarket Submissions

Submission Number Supplement Number
K192314 000