Primary Device ID | B707128300080020 |
NIH Device Record Key | 8bf52830-9611-4b17-9cd8-96ce826ec5b2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DUALX LLIF LOCKOUT SCREW 45MM |
Version Model Number | 12830008002 |
Company DUNS | 081021000 |
Company Name | AMPLIFY SURGICAL, INC. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com | |
Phone | 7652675439 |
udi@amplifysurgical.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B707128300080020 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-05-08 |
B70712830008002A0 | DUALX LLIF LOCKOUT SCREW 45MM |
B707128300080020 | DUALX LLIF LOCKOUT SCREW 45MM |