510(k) K052533
K052533 is an FDA 510(k) premarket notification submitted by Signus Medizintechnik GmbH for the device "KIMBA SPINAL IMPLANT". The FDA issued a decision of Substantially Equivalent on November 3, 2005. The device falls under product code MQP (Spinal Vertebral Body Replacement Device), a Class II device regulated under 21 CFR 888.3060. Signus Medizintechnik GmbH has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 3, 2005
- Date Received
- September 15, 2005
- 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