| Primary Device ID | 04546540756800 |
| NIH Device Record Key | 9abcbf9c-77c5-450e-b96a-c66faf6cef10 |
| Commercial Distribution Discontinuation | 2018-12-07 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Cross-Screw |
| Version Model Number | 234-500-201 |
| Catalog Number | 234-500-201 |
| Company DUNS | 187502109 |
| Company Name | STRYKER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540756800 [Primary] |
| FSM | TRAY, SURGICAL, INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
[04546540756800]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2018-12-07 |
| Device Publish Date | 2015-09-04 |
| 04546540756800 | TRAY BASE FOR CROSS-SCREW INSTRUMENTATION SET |
| 04546540756787 | 8MM X 60MM CROSS-SCREW TITANIUM |
| 04546540756770 | 8MM X 50MM CROSS-SCREW TITANIUM |
| 04546540756763 | 8MM X 40MM CROSS-SCREW TITANIUM |