| Primary Device ID | 08800039102216 |
| NIH Device Record Key | 4e9d662c-4060-483a-9d19-2f446582713f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fixone Hybrid Anchor |
| Version Model Number | KAPN-47501nc |
| Company DUNS | 963422810 |
| Company Name | AJU PHARM. CO., LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800039102216 [Primary] |
| MAI | Fastener, Fixation, Biodegradable, Soft Tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-14 |
| Device Publish Date | 2025-01-06 |
| 08800039102254 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
| 08800039102216 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
| 08800039101035 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
| 08800039101028 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
| 08800039100601 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |
| 08800039100571 | The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. |