| Primary Device ID | M06760001200 |
| NIH Device Record Key | 739df25c-f9f6-4036-9e4f-89a0946d4c52 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integrity Delivery Instrument, Tissue Tack |
| Version Model Number | 6000120 |
| Company DUNS | 807613393 |
| Company Name | Anika Therapeutics, Inc. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M06760001200 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-22 |
| Device Publish Date | 2023-11-14 |
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