FDA UDI In Commercial Distribution 🇺🇸 United States

OZARK Cervical Plate System

DI: 10888857392304 · Model: 8801-14010DA · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OZARK Cervical Plate System
Primary DI
10888857392304
Version / Model
8801-14010DA
Catalog Number
8801-14010DA
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-01
Public Version
5
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
0af62780-f546-481b-ae51-c5b2fe4e96ab

Device Description

Fixed Screw, Self-Starting Size Ø4.0x10 mm

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 10888857392304

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 4 Millimeter
Length 10 Millimeter