Last synced on 19 July 2024 at 11:05 pm

ET Abutment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222636
510(k) Type
Traditional
Applicant
Hiossen Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
240 days
Submission Type
Summary

ET Abutment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222636
510(k) Type
Traditional
Applicant
Hiossen Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
240 days
Submission Type
Summary