FDA UDI Not in Commercial Distribution 🇺🇸 United States

CASCADIA™ Interbody System

DI: 10888857259089 · Model: 6101-2162015CP-G2 · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASCADIA™ Interbody System
Primary DI
10888857259089
Version / Model
6101-2162015CP-G2
Catalog Number
6101-2162015CP-G2
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-18
Public Version
5
Public Version Date
2022-04-06
Public Version Status
Update
Public Device Record Key
b686dc2a-a7c2-40ab-a520-377eac11712a
Distribution End Date
2022-04-05

Device Description

Cervical Interbody Size 16x20x15 mm, 0°

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 10888857259089

Customer Contacts

Device Sizes

Type Value Unit Text
Length 16 Millimeter
Height 15 Millimeter
Width 20 Millimeter