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

3I OSSEOTITE CERTAIN DENTAL IMPLANTS

K Number: K063341 · Decision Apr 30, 2007
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
51
Review Days
175

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Basic Information

Device Name
3I OSSEOTITE CERTAIN DENTAL IMPLANTS
K Number
K063341
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implant Innovations, Inc.
Date Received
November 6, 2006
Decision Date
April 30, 2007
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 Implant Innovations, Inc.

K Number Device Name
K062636 OSSEOTITE, OSSEOTITE NY, CERTAIN, CERTAIN NT, PREVAIL, CERTAIN PREVAIL, XP, MICROMINIPLANT, DENTAL IMPLANTS
K063286 OSSEOTITE; OSSEOTITE NT; XP; TG OSSEOTITE
K063403 CONICAL ANGLED ABUTMENT
K061629 CERTAIN PREVAIL DENTAL IMPLANT
K062432 NANOTITE DENTAL IMPLANTS
K061969 PREFORMANCE POSTS AND TEMPORARY CYLINDERS
K061177 PROVIDE TEMPORARY CYLINDER
K060291 PREFORMANCE TEMPORARY CYLINDER
K053170 PREFORMANCE POSTS
K052648 MODIFICATION TO 3I PATIENT-SPECIFIC DENTAL ABUTMENTS AND OVERDENTURE BARS
Search all 51 clearances from Implant Innovations, Inc. →