Primary Device ID | M7406804652 |
NIH Device Record Key | ad85407f-39d4-4f13-b584-f8cdcc45c751 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ConneX Cross Connector |
Version Model Number | 10-10-82-6 |
Catalog Number | 680-4652 |
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)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com | |
Phone | +1(651)259-8500 |
info@spineology.com |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Size Text, specify | 0 |
Length | 46 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7406804652 [Primary] |
MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
[M7406804652]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-07-22 |
Device Publish Date | 2017-04-25 |
M7406806590 | Cross Connector, Adjustable |
M7406805265 | Cross Connector, Adjustable |
M7406804652 | Cross Connector, Adjustable |
M7406804046 | Cross Connector, Adjustable |
M7406803740 | Cross Connector, Adjustable |
M7406803137 | Cross Connector, Adjustable |
M7406802531 | Cross Connector, Adjustable |
M7406801800 | Cross Connector, Adjustable |