Primary Device ID | 00815101028934 |
NIH Device Record Key | f6cfe0e0-5d44-409d-8e53-22c1e68f6905 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STALIF C-Ti |
Version Model Number | C165539-3Dc |
Company DUNS | 949024850 |
Company Name | Centinel Spine, 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815101028934 [Primary] |
OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STALIF C-TI 88064523 5725943 Live/Registered |
Centinel Spine, LLC 2018-08-03 |