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

SINGLE TOOT ABUTMENT SYSTEM (STA OR ST ABUTMENT ) FOR SINGLE OOTH CEMENT RETAINED RESTORATIONS

K Number: K965077 · Decision Mar 17, 1997
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
51
Review Days
90

Basic Information

Device Name
SINGLE TOOT ABUTMENT SYSTEM (STA OR ST ABUTMENT ) FOR SINGLE OOTH CEMENT RETAINED RESTORATIONS
K Number
K965077
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
December 17, 1996
Decision Date
March 17, 1997
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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Other Clearances by IMPLANT INNOVATIONS, INC.

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K063341 3I OSSEOTITE CERTAIN 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
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