Last synced on 21 June 2024 at 11:04 pm

Osstem Abutment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221684
510(k) Type
Traditional
Applicant
Osstem Implant Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/8/2022
Days to Decision
90 days
Submission Type
Summary

Osstem Abutment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221684
510(k) Type
Traditional
Applicant
Osstem Implant Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/8/2022
Days to Decision
90 days
Submission Type
Summary