Last synced on 25 January 2026 at 3:41 am

SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022065
510(k) Type
Traditional
Applicant
Sintea Biotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2002
Days to Decision
42 days
Submission Type
Summary

SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022065
510(k) Type
Traditional
Applicant
Sintea Biotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2002
Days to Decision
42 days
Submission Type
Summary