510(k) K070316
K070316 is an FDA 510(k) premarket notification submitted by Rsb Spine, LLC for the device "INTERPLATE VBR SYSTEM". The FDA issued a decision of Substantially Equivalent on Apr 19, 2007. The device falls under product code MQP (Spinal Vertebral Body Replacement Device), a Class II device regulated under 21 CFR 888.3060. Rsb Spine, LLC has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 19, 2007
- Date Received
- Feb 1, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Spinal Vertebral Body Replacement Device
- Device Class
- Class II
- Regulation Number
- 888.3060
- Review Panel
- OR
- Submission Type
- 510(k)