Primary Device ID | 00817329021773 |
NIH Device Record Key | d130e5ac-e00b-4c9d-87e2-5b0d14735f58 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VertebraLINK |
Version Model Number | 84-0007/0800 |
Catalog Number | 84-0007/0800 |
Company DUNS | 067584601 |
Company Name | LINKSPINE, INC. |
Device Count | 1 |
DM Exempt | false |
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 | 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 | 1-410-772-5465 |
cs@linkspine.com | |
Phone | 1-410-772-5465 |
cs@linkspine.com | |
Phone | 1-410-772-5465 |
cs@linkspine.com |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817329021773 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-11-28 |
Device Publish Date | 2017-05-18 |
00817329025894 | 8 x 26 x 6 x 6 PLIF IBD |
00817329025887 | 300mm Lordotic Trial 13mm |
00817329025870 | 300mm Lordotic Trial 12mm |
00817329025863 | 300mm Lordotic Trial 11mm |
00817329025856 | 300mm Lordotic Trial 10mm |
00817329025849 | 300mm Lordotic Trial 9mm |
00817329025832 | 300mm Lordotic Trial 8mm |
00817329025825 | 300mm Lordotic Trial 7mm |
00817329025665 | VertebraLINK Set |
00817329025603 | 300mm Trials |
00817329025597 | 300mm Trials |
00817329025580 | 300mm Trials |
00817329025573 | 300mm Trials |
00817329025566 | 300mm Trials |
00817329025559 | 300mm Trials |
00817329025542 | 300mm Trials |
00817329025535 | 300mm Trials |
00817329025528 | 300mm Spreader Shavers |
00817329025511 | 300mm Spreader Shavers |
00817329025504 | 300mm Spreader Shavers |
00817329025498 | 300mm Spreader Shavers |
00817329025481 | 300mm Spreader Shavers |
00817329025474 | 300mm Spreader Shavers |
00817329025467 | 300mm Spreader Shavers |
00817329025450 | 300mm Spreader Shavers |
00817329025443 | 300mm Pituitaries |
00817329025436 | 300mm Pituitaries |
00817329025429 | 300mm Pituitaries |
00817329025412 | 300mm Pituitaries |
00817329025405 | 300mm Pituitaries |
00817329025399 | 300mm Pituitaries |
00817329025382 | 300mm Curette |
00817329025375 | 300mm Curette |
00817329025368 | 300mm Curette |
00817329025351 | 300mm Curette |
00817329025344 | 300mm Curette |
00817329025337 | 300mm Curette |
00817329025320 | VertebraLINK Disc Prep Tray 3 |
00817329025313 | VertebraLINK Posterior Disc Prep Tray 2 |
00817329025306 | VertebraLINK Posterior Disc Prep Tray 1 |
00817329025290 | VertebraLINK Insertion Tray |
00817329025283 | VertebraLINK Prep Tray 1 |
00817329025276 | 300mm Kerrisons |
00817329025269 | 300mm Kerrisons |
00817329025252 | Angled Ring Curette 300mm |
00817329025245 | Angled Ring Curette 300mm |
00817329025238 | 300mm Angled Ring Curette |
00817329025221 | 300mm Angled Ring Curette |
00817329025214 | 300mm Ring Curette |
00817329025207 | Ring Curette 300mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VERTEBRALINK 87382969 5449831 Live/Registered |
LINKSPINE, INC. 2017-03-23 |
VERTEBRALINK 85956547 not registered Dead/Abandoned |
Facet-Link, Inc. 2013-06-11 |