| Primary Device ID | 37613252518403 |
| NIH Device Record Key | bc7d9963-a491-4251-a38e-004939d90197 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5450815114 |
| Catalog Number | 5450815114 |
| Company DUNS | 196548481 |
| Company Name | STRYKER 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 |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613252518402 [Primary] |
| GS1 | 37613252518403 [Package] Contains: 07613252518402 Package: pack [5 Units] In Commercial Distribution |
| LFL | Instrument, ultrasonic surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
| 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 |