FDA UDI Not in Commercial Distribution 🇺🇸 United States

OZARK Cervical Plate System

DI: 10888857360693 · Model: 8801-43F39 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OZARK Cervical Plate System
Primary DI
10888857360693
Version / Model
8801-43F39
Catalog Number
8801-43F39
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-12
Public Version
5
Public Version Date
2023-09-06
Public Version Status
Update
Public Device Record Key
4dbae1e5-ed0d-4007-b5a8-ed0da1c2141f
Distribution End Date
2018-04-23

Device Description

Plate, 3 Level, Size 39 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 10888857360693

Customer Contacts

Device Sizes

Type Value Unit Text
Length 39 Millimeter