Primary Device ID | M7405302030 |
NIH Device Record Key | 58e31961-e08d-400f-8aae-68e476492e26 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Threshold Curved Rod |
Version Model Number | 10-10-07-23 |
Catalog Number | 530-2030 |
Company DUNS | 033014361 |
Company Name | SPINEOLOGY INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com | |
Phone | +1(651)256-8500 |
info@spineology.com |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Length | 30 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7405302030 [Primary] |
MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
[M7405302030]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-07-23 |
Device Publish Date | 2015-01-09 |
M7405304200 | Long Fixed Rods |
M7405304180 | Long Fixed Rods |
M7405304160 | Long Fixed Rods |
M7405304140 | Long Fixed Rods |
M7405302120 | Curved Rod |
M7405302110 | Curved Rod |
M7405302100 | Curved Rod |
M7405302090 | Curved Rod |
M7405302080 | Curved Rod |
M7405302075 | Curved Rod |
M7405302070 | Curved Rod |
M7405302065 | Curved Rod |
M7405302060 | Curved Rod |
M7405302055 | Curved Rod |
M7405302050 | Curved Rod |
M7405302045 | Curved Rod |
M7405302040 | Curved Rod |
M7405302035 | Curved Rod |
M7405302030 | Curved Rod |