Primary Device ID | M719ACC1050 |
NIH Device Record Key | c778be1f-7e66-49cb-a538-36c8d79883ab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AIS-C II |
Version Model Number | 1 |
Catalog Number | ACC105 |
Company DUNS | 017921066 |
Company Name | Genesys Orthopedics Systems LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com | |
Phone | 5123817070 |
info@genesysspine.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M719ACC1050 [Primary] |
OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
[M719ACC1050]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-12 |
Device Publish Date | 2024-03-04 |
M719ACC1060 | AIS-C II Impaction Inserter, Threaded |
M719ACC1050 | AIS-C II Impaction Inserter |
M719ACC1040 | AIS-C II Gun Inserter |
M719ACC1030 | AIS-C II Anchor Extractor |