| Primary Device ID | 07613327354102 |
| NIH Device Record Key | 121e005f-bd68-4769-9a5c-9d36b0606d55 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 2781 |
| Catalog Number | 2781-100-000 |
| Company DUNS | 078470558 |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 07613327354102 [Primary] |
| IOQ | BED, FLOTATION THERAPY, POWERED |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
| 07613327627664 - KNOTILUS+ | 2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK |
| 07613327627701 - KNOTILUS+ | 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK |
| 07613327623796 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HIP |
| 07613327623833 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP |
| 07613327634686 - Iconix | 2024-03-12 Iconix DC Guide for 1.4mm anchor |
| 07613327634693 - Iconix | 2024-03-12 |
| 07613327616675 - SPY | 2024-03-06 |
| 07613327616682 - SPY | 2024-03-06 |