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

DENTAL IMPLANT SYSTEM 4.0MM AND 5.5MM LENGTH

K Number: K912521 · Decision May 2, 1995
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
1440

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Basic Information

Device Name
DENTAL IMPLANT SYSTEM 4.0MM AND 5.5MM LENGTH
K Number
K912521
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bud Industries, Inc.
Date Received
May 23, 1991
Decision Date
May 2, 1995
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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Other Clearances by Bud Industries, Inc.

K Number Device Name
K913688 BUD MAXILLOFACIAL IMPLANT SYSTEM
K902331 BUD DENTAL IMPLANT SYSTEM