FDA UDI In Commercial Distribution 🇺🇸 United States

Alamo C Interbody Fusion Device

DI: M6861714I7100 · Model: 1714I-710 · ALLIANCE PARTNERS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alamo C Interbody Fusion Device
Primary DI
M6861714I7100
Version / Model
1714I-710
Catalog Number
1714I-710
Company Name
ALLIANCE PARTNERS LLC
Labeler DUNS
962768169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-03
Public Version
5
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
79a173ad-28d2-4e80-b3d6-8ebc86f1616e

Device Description

Cervical Interbody Fusion Device, PEEK

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
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M6861714I7100

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133321 000

Device Sizes

Type Value Unit Text
Angle 7 degree
Height 10 Millimeter
Width 17 Millimeter
Length 14 Millimeter