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

CONAGRAF TM DURAPATITE CONES

K Number: K820023 · Decision Feb 24, 1982
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
9
Review Days
50

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Basic Information

Device Name
CONAGRAF TM DURAPATITE CONES
K Number
K820023
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sterling Drug, Inc.
Date Received
January 5, 1982
Decision Date
February 24, 1982
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

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K875275 WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER
K840260 PERIOGRAF DURAPATITE 40-60 MESH
K820164 EMPTY STERILE CARPUJECT
K813257 ALVEOGRAF DURAPATITE(18-40 MESH)
K813070 PERIOGRAF
K780209 DILUTION SPIKE