FDA UDI In Commercial Distribution 🇺🇸 United States

ALEUTIAN® Interbody Systems

DI: 10888857116276 · Model: 602-90319 · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ALEUTIAN® Interbody Systems
Primary DI
10888857116276
Version / Model
602-90319
Catalog Number
602-90319
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
cf47d1d5-9253-4ab2-9cd8-7b7136a4f769

Device Description

Convex Trial, Size 8.5x28x11 mm

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
ODP Intervertebral fusion device with bone graft, cervical
MAX Intervertebral fusion device with bone graft, lumbar
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10888857116276

Customer Contacts

Device Sizes

Type Value Unit Text
Length 28 Millimeter
Height 11 Millimeter
Width 8.5 Millimeter