Primary Device ID | 00840996163804 |
NIH Device Record Key | 79ee97b1-ca66-43ce-987c-28f76b2b49cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Octane Straight IR |
Version Model Number | PT23-32156 |
Company DUNS | 078293017 |
Company Name | Choice Spine, LP |
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 | 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 | +1(865)246-3333 |
info@choicespine.net |
Width | 32 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840996163804 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840996163804]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2017-09-20 |
00840996163804 | OCTANE STRAIGHT IR, Ti, 32X10X15, 6 DEG |
00840996163798 | OCTANE STRAIGHT IR, Ti, 32X10X14, 6 DEG |
00840996163781 | OCTANE STRAIGHT IR, Ti, 32X10X13, 6 DEG |
00840996163774 | OCTANE STRAIGHT IR, Ti, 32X10X12, 6 DEG |
00840996163767 | OCTANE STRAIGHT IR, Ti, 32X10X11, 6 DEG |
00840996163750 | OCTANE STRAIGHT IR, Ti, 36X10X15, 6 DEG |
00840996163743 | OCTANE STRAIGHT IR, Ti, 36X10X14, 6 DEG |
00840996163736 | OCTANE STRAIGHT IR, Ti, 36X10X13, 6 DEG |
00840996163729 | OCTANE STRAIGHT IR, Ti, 36X10X12, 6 DEG |
00840996163712 | OCTANE STRAIGHT IR, Ti, 36X10X11, 6 DEG |