FDA UDI Not in Commercial Distribution 🇺🇸 United States

OZARK Cervical Plate System

DI: 10888857354012 · Model: 8801-04313C · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OZARK Cervical Plate System
Primary DI
10888857354012
Version / Model
8801-04313C
Catalog Number
8801-04313C
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
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a94976a2-f14b-4e3e-97cc-4bc631d983dc
Distribution End Date
2018-04-23

Device Description

Self-Tapping, Variable Screw, Size Ø4.35x13 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 10888857354012

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K172104 000

Device Sizes

Type Value Unit Text
Length 13 Millimeter
Outer Diameter 4.35 Millimeter