Last synced on 25 January 2026 at 3:41 am

IM/ST Fixture System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212702
510(k) Type
Traditional
Applicant
Guilin Fiteeth Medical Instrument Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
413 days
Submission Type
Summary

IM/ST Fixture System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212702
510(k) Type
Traditional
Applicant
Guilin Fiteeth Medical Instrument Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
413 days
Submission Type
Summary