Primary Device ID | 00190376115955 |
NIH Device Record Key | a23439a5-080e-4695-9f04-59e885535b47 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aspida |
Version Model Number | 51101-24 |
Company DUNS | 602465783 |
Company Name | ALPHATEC SPINE, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Height | 24 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190376115955 [Primary] |
KWQ | Appliance, fixation, spinal intervertebral body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
[00190376115955]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-16 |
Device Publish Date | 2019-11-06 |
00840967190846 | TEMPORARY FIXATION PIN |
00190376159645 | Medial Temporary Fixation Pin |
00190376159638 | 24MM SACRAL PLATE |
00190376159621 | 22MM SACRAL PLATE |
00190376159614 | 20MM SACRAL PLATE |
00190376159607 | 24MM LUMBAR PLATE |
00190376159591 | 22MM LUMBAR PLATE |
00190376159584 | 20MM LUMBAR PLATE |
00190376116044 | 24mm SACRAL PLATE, TF |
00190376116037 | 22mm SACRAL PLATE, TF |
00190376116020 | 20mm SACRAL PLATE, TF |
00190376116013 | 18mm SACRAL PLATE, TF |
00190376116006 | 16mm SACRAL PLATE, TF |
00190376115993 | 14mm SACRAL PLATE, TF |
00190376115986 | 12mm SACRAL PLATE, TF |
00190376115979 | 10mm SACRAL PLATE, TF |
00190376115955 | 24mm LUMBAR PLATE, TF |
00190376115948 | 22mm LUMBAR PLATE, TF |
00190376115931 | 20mm LUMBAR PLATE, TF |
00190376115924 | 18mm LUMBAR PLATE,TF |
00190376115917 | 16mm LUMBAR PLATE,TF |
00190376115900 | 14mm LUMBAR PLATE, TF |
00190376115894 | 12mm LUMBAR PLATE, TF |
00190376115887 | 10mm LUMBAR PLATE, TF |
00190376115962 | 8mm SACRAL PLATE, TF |
00190376115870 | 8mm LUMBAR PLATE, TF |
00190376275239 | ASPIDA Anterior Lumbar Plate System, TF |
00190376275222 | ASPIDA ANTERIOR LUMBAR PLATE |
00844856037083 | PLATE HOLDER |
00811801039706 | Aspida Plate Holder - Threaded Lock |
00844856037090 | SELF CENTERING AWL |
00811801038358 | Adjustable ASPIDA Awl Guide |
00811801038341 | Adjustable ASPIDA Awl |
00190376470382 | ASPIDA Anterior Lumbar Plate System - Condensed |
00844856037120 | TAP |
00840967190891 | DTS TAP |
00811801037757 | Aspida Temp Tack Driver and Sleeve |
00190376000039 | Aspida Stab and Grab Inserter 2.0 |
00840967190877 | SCREW REMOVAL TOOL |
00811801037450 | Aspida Stab and Grab Inserter |
00811801035241 | Sleeveless Aspida Screw Removal Tool |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ASPIDA 98328087 not registered Live/Pending |
LAB 394, LLC 2023-12-22 |
![]() ASPIDA 98068537 not registered Live/Pending |
Buckeye International, Inc. 2023-07-02 |
![]() ASPIDA 90717436 not registered Live/Pending |
LEKKAKIS PETROS 2021-05-18 |
![]() ASPIDA 88515706 not registered Live/Pending |
Ares Management LLC 2019-07-15 |
![]() ASPIDA 88207159 not registered Live/Pending |
Buckeye International, Inc. 2018-11-27 |
![]() ASPIDA 85067995 4088638 Dead/Cancelled |
Alphatec Spine, Inc. 2010-06-21 |
![]() ASPIDA 77309700 3533285 Dead/Cancelled |
Aspida Oy 2007-10-22 |