FDA UDI In Commercial Distribution 🇺🇸 United States

Alamo P Interbody Fusion Device

DI: M6862210I7100 · Model: 2210I-710 · ALLIANCE PARTNERS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alamo P Interbody Fusion Device
Primary DI
M6862210I7100
Version / Model
2210I-710
Catalog Number
2210I-710
Company Name
ALLIANCE PARTNERS LLC
Labeler DUNS
962768169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
33c990ee-1a89-4612-8821-26b663888a82

Device Description

Posterior Lumbar 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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M6862210I7100

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122047 000

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Angle 7 degree
Width 10 Millimeter
Height 10 Millimeter