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

ITI ANGLED ABUTMENT

K Number: K941393 · Decision Jun 14, 1995
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
449

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ITI ANGLED ABUTMENT
K Number
K941393
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
March 22, 1994
Decision Date
June 14, 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.

View all

Other Clearances by The Straumann Co.

K Number Device Name
K041070 STRAUMANN TEMPORARY COPING
K040646 STRAUMANN GRANULES
K040469 THE STRAUMANN ORTHO IMPLANT SYSTEM
K993862 MODUS SAGITTAL SPLIT PLATE
K962023 PLASTIC PROTECTION HEALING CAPS
K960634 TITANIUM HEALING CAPS
K955281 ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
K955369 MEMFIX
K943720 ITI TRANSVERSAL SCREWING SYSTEM
K931993 ITI DISTANCE SYSTEM
Search all 14 clearances from The Straumann Co. →