Last synced on 18 April 2025 at 11:05 pm

IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932123
510(k) Type
Traditional
Applicant
IMPLANT INNOVATIONS INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1994
Days to Decision
389 days
Submission Type
Summary

IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932123
510(k) Type
Traditional
Applicant
IMPLANT INNOVATIONS INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/1994
Days to Decision
389 days
Submission Type
Summary