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

BIOLITE CARBON COATED DENTAL IMPLANT

K Number: K791491 · Decision Sep 4, 1979
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
22
Review Days
29

Basic Information

Device Name
BIOLITE CARBON COATED DENTAL IMPLANT
K Number
K791491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
CARBOMEDICS, INC.
Date Received
August 6, 1979
Decision Date
September 4, 1979
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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