| Primary Device ID | 20845854016463 |
| NIH Device Record Key | 259a2cdd-3e20-410d-823e-d3d288024a65 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | C8952 |
| Catalog Number | C8952 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Length | 30 Millimeter |
| Outer Diameter | 8 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854016463 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
[20845854016463]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 30653405990486 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 15MM, TITANIUM |
| 30653405990493 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 20MM, TITANIUM |
| 30653405990509 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 15MM, TITANIUM |
| 30653405990516 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 20MM, TITANIUM |
| 30653405990523 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 30MM, TITANIUM |
| 30653405990530 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 15MM, TITANIUM |
| 30653405990547 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 20MM, TITANIUM |
| 30653405990554 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 25MM, TITANIUM |