FDA UDI In Commercial Distribution 🇺🇸 United States

ALEUTIAN® Interbody Systems

DI: 10888857092013 · Model: 403-22012L · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ALEUTIAN® Interbody Systems
Primary DI
10888857092013
Version / Model
403-22012L
Catalog Number
403-22012L
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
2023-07-31
Public Version Status
Update
Public Device Record Key
7cde0492-d565-4af6-b9af-515b4514b7c6

Device Description

Lordotic Implant

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

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 10888857092013

Customer Contacts

Device Sizes

Type Value Unit Text
Width 12.5 Millimeter
Angle 7 degree
Height 12 Millimeter
Length 20 Millimeter