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

VITABLOCS, MODEL VX55-****

K Number: K090644 · Decision Mar 31, 2009
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
6
Review Days
21

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Basic Information

Device Name
VITABLOCS, MODEL VX55-****
K Number
K090644
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vita Zahnfabrik H.Rauter GmbH & Co.
Date Received
March 10, 2009
Decision Date
March 31, 2009
Product Code
EIH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EIH Powder, Porcelain

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Other Clearances by Vita Zahnfabrik H.Rauter GmbH & Co.

K Number Device Name
K243940 VITA YZ Multi Translucent
K152373 VITA VM LC Flow
K132070 VITA SUPRINITY(R)
K122269 ENAMIC
K102128 VITABLOCS