FDA UDI In Commercial Distribution 🇺🇸 United States

Blue Ridge Hybrid Cervical Plate System

DI: 10888857084971 · Model: 3914-41F28 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Blue Ridge Hybrid Cervical Plate System
Primary DI
10888857084971
Version / Model
3914-41F28
Catalog Number
3914-41F28
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2023-09-12
Public Version Status
Update
Public Device Record Key
dc8fda43-bcba-4d13-82a7-2778763038f7

Device Description

Constrained Plate, 1 Level

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 10888857084971

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Level
Length 28 Millimeter