FDA UDI In Commercial Distribution 🇺🇸 United States

CASCADIA™ Interbody System

DI: 10888857316645 · Model: 6101-2102405NL12-G2 · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASCADIA™ Interbody System
Primary DI
10888857316645
Version / Model
6101-2102405NL12-G2
Catalog Number
6101-2102405NL12-G2
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-15
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
45ad357a-ae31-45ec-a388-4fc7100d343c

Device Description

AN Interbody, Size 10x24x5 mm, 12 Deg.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 10888857316645

Customer Contacts

Device Sizes

Type Value Unit Text
Height 5 Millimeter
Length 24 Millimeter
Width 10 Millimeter
Angle 12 degree