Primary Device ID | M7405302100 |
NIH Device Record Key | 7ef56bd6-9419-4f9d-8c45-97ff6b633528 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Threshold Curved Rod |
Version Model Number | 10-10-08-14 |
Catalog Number | 530-2100 |
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 | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Length | 100 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7405302100 [Primary] |
NKB | Orthosis, spinal pedicle fixation, for degenerative disc disease |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
Ethylene Oxide
[M7405302100]
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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M7405302045 | Curved Rod |
M7405302040 | Curved Rod |
M7405302035 | Curved Rod |
M7405302030 | Curved Rod |