FDA UDI In Commercial Distribution 🇺🇸 United States

Hyper-C Anterior Cervical Plate System

DI: 00842048106968 · Model: 0203-4516F · DEGEN MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hyper-C Anterior Cervical Plate System
Primary DI
00842048106968
Version / Model
0203-4516F
Catalog Number
0203-4516F
Company Name
DEGEN MEDICAL, INC.
Labeler DUNS
078812602
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
13add6e2-c5bf-440f-8fca-65addff931c9

Device Description

Bone Screw, Self Drilling, 4.6 X 16 Fixed

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00842048106968

Premarket Submissions

Submission Number Supplement Number
K150759 000

Device Sizes

Type Value Unit Text
Length 16 Millimeter
Outer Diameter 4.6 Millimeter