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

VITALLIUM EQUIPOISE ALLOY

K Number: K880875 · Decision Apr 7, 1988
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
19
Review Days
37

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Basic Information

Device Name
VITALLIUM EQUIPOISE ALLOY
K Number
K880875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Austenal Dental, Inc.
Date Received
March 1, 1988
Decision Date
April 7, 1988
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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Other Clearances by Austenal Dental, Inc.

K Number Device Name
K890713 OVERDENTURE - STUD ATTACHMENT
K883799 BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN
K871849 LIGHT CURE DENTURE GLAZE
K872746 VITALLIUM WIRE
K863630 AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
K862557 AUSTENAL ACUSOFT SOFT LINER
K865025 AUSTENAL CONDENSING INSTRUMENT
K864826 A-SP ALLOY (SILVER-PALLADIUM CROWN & BRIDGE ALLOY)
K862856 PALLADIUM BASED DENT ALLOYS/PORCELAIN METAL RESTOR
K862667 COBALT, 29.5% CHROMIUM ALLOY DENTAL BAKE-ON ALLOY
Search all 19 clearances from Austenal Dental, Inc. →