| Primary Device ID | 00817893020684 |
| NIH Device Record Key | 3af7f048-ade0-4a1f-921c-9ce0acc55026 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InterPlate® |
| Version Model Number | C-Ti |
| Catalog Number | RSB433 |
| Company DUNS | 038558909 |
| Company Name | RSB 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817893020684 [Primary] |
| HXX | Screwdriver |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00817893020684]
Moist Heat or Steam Sterilization
[00817893020684]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2018-10-05 |
| Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() INTERPLATE 78938581 3309930 Live/Registered |
RSB Spine LLC 2006-07-27 |
![]() INTERPLATE 75149939 2211509 Dead/Cancelled |
PerSeptive Biosystems, Inc. 1996-08-14 |
![]() INTERPLATE 73377432 1250782 Dead/Cancelled |
Occidental Chemical Corporation 1982-07-30 |
![]() INTERPLATE 73129348 1083085 Live/Registered |
INTERNATIONAL PAINT COMPANY, INC. 1977-06-06 |
![]() INTERPLATE 72439304 0974522 Dead/Expired |
VERSA PRODUCTS COMPANY, INC. 1972-10-25 |