FDA 510(k) Applications Submitted by Rubicon Spine, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181030 | 04/18/2018 | Rubicon Lumbar Interbody Fusion System | Rubicon Spine, LLC |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact