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

ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

K Number: K971196 · Decision May 8, 1997
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
6
Review Days
38

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Basic Information

Device Name
ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM
K Number
K971196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innova Corp.
Date Received
March 31, 1997
Decision Date
May 8, 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 Innova Corp.

K Number Device Name
K040714 HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT
K984117 INNOVA TELESCOPIC DISTRACTOR
K952434 ENDOPORE DENTAL IMPLANT ABUTMENTS
K926354 ENDO-PORE ENDOSSEOUS DENTAL IMPLANT SYSTEM
K915361 THE BODY BUGGY