FDA UDI In Commercial Distribution 🇺🇸 United States

Suzuka Interbody Fusion System

DI: B417ALR170081 · Model: ALR17-008 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Suzuka Interbody Fusion System
Primary DI
B417ALR170081
Version / Model
ALR17-008
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-22
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
25cfb503-612d-446f-b32f-80d4d50dcf3a

Device Description

Interbody Fusion Device, PEEK ALR, 17x13.5, 8mm 0degree

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
Yes
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

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B417ALR170081
Secondary 00843210107097

Customer Contacts

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Length 13.5 Millimeter
Width 17 Millimeter