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

NOBEL DIRECT, MODELS 30937, 30938

K Number: K031345 · Decision Jul 24, 2003
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
31
Review Days
86

Basic Information

Device Name
NOBEL DIRECT, MODELS 30937, 30938
K Number
K031345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOBEL BIOCARE UAS INC
Date Received
April 29, 2003
Decision Date
July 24, 2003
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

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