FDA UDI In Commercial Distribution 🇺🇸 United States

CASCADIA™ Interbody System

DI: 10888857383661 · Model: 7902-90013 · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASCADIA™ Interbody System
Primary DI
10888857383661
Version / Model
7902-90013
Catalog Number
7902-90013
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-30
Public Version
3
Public Version Date
2023-09-13
Public Version Status
Update
Public Device Record Key
e873be08-dd04-4fb5-be61-78ed551595ba

Device Description

Lateral Trial, Size 22x50x18 mm 28 Deg.

Device Characteristics

Single Use
No
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
OVD Intervertebral fusion device with integrated fixation, lumbar
ODP Intervertebral fusion device with bone graft, cervical
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10888857383661

Customer Contacts

Device Sizes

Type Value Unit Text
Length 50 Millimeter
Height 18 Millimeter
Width 22 Millimeter