Primary Device ID | M7405304050 |
NIH Device Record Key | e9af220f-d805-41c3-a318-85256d966938 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Threshold Fixed Perc Rod |
Version Model Number | 10-10-07-5 |
Catalog Number | 530-4050 |
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 | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Length | 50 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7405304050 [Primary] |
NKB | Orthosis, spinal pedicle fixation, for degenerative disc disease |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
Ethylene Oxide
[M7405304050]
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 |
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M7405304110 | Fixed Perc Rod |
M7405304100 | Fixed Perc Rod |
M7405304095 | Fixed Perc Rod |
M7405304090 | Fixed Perc Rod |
M7405304085 | Fixed Perc Rod |
M7405304080 | Fixed Perc Rod |
M7405304075 | Fixed Perc Rod |
M7405304070 | Fixed Perc Rod |
M7405304065 | Fixed Perc Rod |
M7405304060 | Fixed Perc Rod |
M7405304055 | Fixed Perc Rod |
M7405304050 | Fixed Perc Rod |
M7405304045 | Fixed Perc Rod |
M7405304040 | Fixed Perc Rod |
M7405304035 | Fixed Perc Rod |
M7405304030 | Fixed Perc Rod |