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

VBB SYSTEM

K Number: K110604 · Decision Dec 13, 2011
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
107
Applicant Total
11
Review Days
285

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Basic Information

Device Name
VBB SYSTEM
K Number
K110604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes
Date Received
March 3, 2011
Decision Date
December 13, 2011
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

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Other Clearances by Synthes

K Number Device Name
K123723 SYNTHES MATRIXNEURO CRANIAL PLATING SYSTEM
K122455 SYNTHES SMALL EXTERNAL FIXATION SYSTEM, SYNTHES LARGE EXTERNAL FIXATION SYSTEM
K113071 SYNTHECEL DURA REPLACEMENT DEVICES
K093772 SYNTHES STERNAL FIXATION SYSTEM
K013072 CHRONOS TRICALCIUM PROSPHATE (CHRONOS TCP)
K020602 SYNTHES PILON PLATE
K010108 USS-LINE EXTENSION
K003836 SYNTHES SYNEX SPACER SYSTEM
K003061 SYNTHES USS (10.0MM SIDE OPENING SCREWS)
K982732 SYNTHES (USA) DISTAL RADIUS PLATE SYSTEM (DRPS)
Search all 11 clearances from Synthes →