Primary Device ID | 00880304982444 |
NIH Device Record Key | 9109fcda-1d8c-4b00-ab8c-24002330b8fe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Solitaire®-C Cervical Spacer |
Version Model Number | 14-531727E |
Catalog Number | 14-531727E |
Company DUNS | 018577570 |
Company Name | BIOMET SPINE LLC |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304982444 [Primary] |
OVE | Intervertebral fusion device with integrated fixation, cervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-03 |
Device Publish Date | 2020-06-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SOLITAIRE 98469468 not registered Live/Pending |
Guru Smart Holding Limited 2024-03-26 |
SOLITAIRE 97638439 not registered Live/Pending |
Rocky Patel Premium Cigars, Inc. 2022-10-19 |
SOLITAIRE 88202496 5935281 Live/Registered |
Hyundai Motor Company 2018-11-21 |
SOLITAIRE 87132277 5124425 Live/Registered |
FINGER ARTS, LLC 2016-08-09 |
SOLITAIRE 87032551 not registered Dead/Abandoned |
Vincent De Tiberiis 2016-05-11 |
SOLITAIRE 86547179 4921188 Live/Registered |
Arnold, Olga 2015-02-26 |
SOLITAIRE 86047961 4545248 Live/Registered |
Mark Ferguson 2013-08-26 |
SOLITAIRE 85923981 4532190 Live/Registered |
Markanna Studios, inc 2013-05-06 |
SOLITAIRE 85897229 not registered Dead/Abandoned |
SONOMA ESTATE VINTNERS, LLC 2013-04-06 |
SOLITAIRE 85783777 4937038 Live/Registered |
Kinetico Incorporated 2012-11-20 |
SOLITAIRE 85308935 not registered Dead/Abandoned |
MONSTER, INC. 2011-04-29 |
SOLITAIRE 85192566 4066003 Live/Registered |
Buck Knives, Inc. 2010-12-07 |