The following data is part of a premarket notification filed by Reliance Medical Systems, Llc with the FDA for Reliance Vbs System.
| Device ID | K063637 |
| 510k Number | K063637 |
| Device Name: | RELIANCE VBS SYSTEM |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | Reliance Medical Systems, LLC 1838 E 9800 SOUTH Sandy, UT 84092 |
| Contact | Bret M Berry |
| Correspondent | Bret M Berry Reliance Medical Systems, LLC 1838 E 9800 SOUTH Sandy, UT 84092 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-12-07 |
| Decision Date | 2007-09-27 |
| Summary: | summary |