510(k) K132817
K132817 is an FDA 510(k) premarket notification submitted by Benvenue Medical, Inc. for the device "KIVA VCF TREATMENT SYSTEM". The FDA issued a decision of Substantially Equivalent on January 24, 2014. The device falls under product code NDN (Cement, Bone, Vertebroplasty), a Class II device regulated under 21 CFR 888.3027. Benvenue Medical, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 2014
- Date Received
- September 9, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cement, Bone, Vertebroplasty
- Device Class
- Class II
- Regulation Number
- 888.3027
- Review Panel
- OR
- Submission Type