FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

PHOENIX 3.25 MM C.P. COATED DENTAL IMPLANT

K Number: K926366 · Decision Sep 21, 1995
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
1003

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Basic Information

Device Name
PHOENIX 3.25 MM C.P. COATED DENTAL IMPLANT
K Number
K926366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
International Implant Seminars
Date Received
December 22, 1992
Decision Date
September 21, 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 International Implant Seminars

K Number Device Name
K926371 ANGLED 3.25 MM DENTAL IMPLANT ATTACHMENTS
K926367 PHOENIX 3.25 MM HA COATED DENTAL IMPLANT
K926370 STRAIGHT 3.25 MM DENTAL IMPLANT ATTACHMENTS