Alamo P Interbody Fusion Device 2210I-010

GUDID M6862210I0100

Posterior Lumbar Interbody Fusion Device, PEEK

ALLIANCE PARTNERS LLC

Polymeric spinal interbody fusion cage
Primary Device IDM6862210I0100
NIH Device Record Key9b50b196-5e04-462a-b14a-28bea45d7b94
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlamo P Interbody Fusion Device
Version Model Number2210I-010
Catalog Number2210I-010
Company DUNS962768169
Company NameALLIANCE PARTNERS LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(210)314-2525
Emailinfo@alliance-spine.com

Device Dimensions

Width10 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM6862210I0100 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M6862210I0100]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-24
Device Publish Date2015-09-14

On-Brand Devices [Alamo P Interbody Fusion Device]

M6862810I7140Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I7130Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I7120Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I7110Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I7100Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I7090Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0140Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0130Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0120Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0110Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0100Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0090Posterior Lumbar Interbody Fusion Device, PEEK
M6862810I0080Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7140Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7130Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7120Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7110Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7100Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I7090Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0140Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0130Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0120Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0110Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0100Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0090Posterior Lumbar Interbody Fusion Device, PEEK
M6862510I0080Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7140Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7130Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7120Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7110Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7100Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I7090Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0140Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0130Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0120Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0110Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0100Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0090Posterior Lumbar Interbody Fusion Device, PEEK
M6862210I0080Posterior Lumbar Interbody Fusion Device, PEEK

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.