| Primary Device ID | M7404105345 |
| NIH Device Record Key | 33e550a5-f5c1-4d64-bae8-96a1c3f3c4e9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CAPTURE |
| Version Model Number | 70-01-002-5 |
| Catalog Number | 410-5345 |
| 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 | 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(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com | |
| Phone | +1(612)256-8500 |
| info@spineology.com |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Length | 45 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M7404105345 [Primary] |
| NKB | Orthosis, spinal pedicle fixation, for degenerative disc disease |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-07-23 |
| Device Publish Date | 2015-10-05 |
| M7404205350 | Capture Facet Screw |
| M7404205345 | Capture Facet Screw |
| M7404205340 | Capture Facet Screw |
| M7404205335 | Capture Facet Screw |
| M7404205330 | Capture Facet Screw |
| M7404205325 | Capture Facet Screw |
| M7404205320 | Capture Facet Screw |
| M7404105350 | Capture Facet Screw |
| M7404105345 | Capture Facet Screw |
| M7404105340 | Capture Facet Screw |
| M7404105335 | Capture Facet Screw |
| M7404105330 | Capture Facet Screw |
| M7404105325 | Capture Facet Screw |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CAPTURE 98432555 not registered Live/Pending |
Verikai Inc. 2024-03-04 |
![]() CAPTURE 97695445 not registered Live/Pending |
Neural DSP Technologies Oy 2022-11-29 |
![]() CAPTURE 97550370 not registered Live/Pending |
Pittman Dental Laboratory 2022-08-16 |
![]() CAPTURE 97549124 not registered Live/Pending |
Forward Beauty Inc. 2022-08-15 |
![]() CAPTURE 97536516 not registered Live/Pending |
CAPTURE COLLECTIVE, INC. 2022-08-05 |
![]() CAPTURE 97536444 not registered Live/Pending |
CAPTURE COLLECTIVE, INC. 2022-08-05 |
![]() CAPTURE 97536344 not registered Live/Pending |
CAPTURE COLLECTIVE, INC. 2022-08-05 |
![]() CAPTURE 97536238 not registered Live/Pending |
CAPTURE COLLECTIVE, INC. 2022-08-05 |
![]() CAPTURE 97113068 not registered Live/Pending |
Carmen Maxwell A 2021-11-08 |
![]() CAPTURE 90976916 not registered Live/Pending |
YesVideo, Inc. 2020-09-14 |
![]() CAPTURE 90723607 not registered Live/Pending |
Ademco Inc. 2021-05-20 |
![]() CAPTURE 90317905 not registered Live/Pending |
Breg, Inc. 2020-11-13 |