FDA UDI In Commercial Distribution 🇺🇸 United States

ALEUTIAN® Interbody Systems

DI: 10888857120594 · Model: 602-90876 · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ALEUTIAN® Interbody Systems
Primary DI
10888857120594
Version / Model
602-90876
Catalog Number
602-90876
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
5
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
df1d7e44-2338-42d1-8eb5-ad1f755083a5

Device Description

Lordotic AN Inserter, Tapered, Size 28 mm - .360, Tapered

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

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10888857120594

Customer Contacts

Device Sizes

Type Value Unit Text
Length 28 Millimeter