| Primary Device ID | 00817577020436 |
| NIH Device Record Key | 07530854-a0c5-4d72-b68d-8005ed2c33b3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EPIC CANNULATED SCREW SYSTEM |
| Version Model Number | A |
| Catalog Number | 1000-5022 |
| Company DUNS | 157565946 |
| Company Name | Exactech, 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 | 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00817577020436 [Primary] |
| HWC | Screw, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00817577020436]
Moist Heat or Steam Sterilization
[00817577020436]
Moist Heat or Steam Sterilization
[00817577020436]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-01-27 |
| Device Publish Date | 2016-09-24 |