FDA 510(k) Applications Submitted by Amplify Surgical Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192434 | 09/05/2019 | DualX Lumbar Intervertebral Body Fusion Device | Amplify Surgical Inc |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact