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

ALVEOGRAF DURAPATITE(18-40 MESH)

K Number: K813257 · Decision Jan 5, 1982
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
9
Review Days
47

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Basic Information

Device Name
ALVEOGRAF DURAPATITE(18-40 MESH)
K Number
K813257
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Sterling Drug, Inc.
Date Received
November 19, 1981
Decision Date
January 5, 1982
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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K840260 PERIOGRAF DURAPATITE 40-60 MESH
K820164 EMPTY STERILE CARPUJECT
K820023 CONAGRAF TM DURAPATITE CONES
K813070 PERIOGRAF
K780209 DILUTION SPIKE