510(k) K071372
K071372 is an FDA 510(k) premarket notification submitted by Rsb Spine, LLC for the device "MODIFICATION TO: INTERPLATE VBR SYSTEM". The FDA issued a decision of Substantially Equivalent on Jun 11, 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
- Jun 11, 2007
- Date Received
- May 16, 2007
- Clearance Type
- Special
- 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)