FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AVAMAX VERTEBRAL BALLOON MODEL VBS1010, VBS1015, VBS1020

K Number: K093463 · Decision Feb 26, 2010
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
107
Applicant Total
34
Review Days
112

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AVAMAX VERTEBRAL BALLOON MODEL VBS1010, VBS1015, VBS1020
K Number
K093463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Care Fusion
Date Received
November 6, 2009
Decision Date
February 26, 2010
Product Code
NDN
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NDN Cement, Bone, Vertebroplasty

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NDN), ordered by most recent decision date.

View all

Other Clearances by Care Fusion

K Number Device Name
K233021 BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access Device
K231888 BD Texium™ Needle-Free Syringe
K221327 BD Alaris™ Pump Infusion Sets
K221319 BD Alaris™ Pump Epidural Infusion Set
K223101 BD Secondary Infusion Set
K223088 BD SmartSite™ Needle-Free Connector
K223076 BD Texium™ Closed Male Luer
K201155 PleurX Peritoneal Catheter System
K170405 BD Curve Ascites Shunt
K171531 Jamshidi Bone Marrow Biopsy/Aspiration Needle, Jamshidi T-Handle Bone Marrow Biopsy/Aspiration Needle, Jamshidi Evolve Bone Marrow Biopsy/Aspiration Needle
Search all 34 clearances from Care Fusion →