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

VITALLIUM 2000 ALLOY; VITALLIUM 2000 PLUS ALLOY; COBALT CHROME CASTING ALLOY

K Number: K970205 · Decision Apr 21, 1997
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
10
Review Days
90

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Basic Information

Device Name
VITALLIUM 2000 ALLOY; VITALLIUM 2000 PLUS ALLOY; COBALT CHROME CASTING ALLOY
K Number
K970205
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Austenal, Inc.
Date Received
January 21, 1997
Decision Date
April 21, 1997
Product Code
EJH
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
EJH Alloy, Metal, Base

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