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

PROVIDE TEMPORARY CYLINDER

K Number: K061177 · Decision May 16, 2006
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
51
Review Days
19

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Basic Information

Device Name
PROVIDE TEMPORARY CYLINDER
K Number
K061177
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implant Innovations, Inc.
Date Received
April 27, 2006
Decision Date
May 16, 2006
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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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
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
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. →