Last synced on 25 January 2026 at 3:41 am

SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041989
510(k) Type
Traditional
Applicant
Sintea Biotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
55 days
Submission Type
Summary

SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041989
510(k) Type
Traditional
Applicant
Sintea Biotech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2004
Days to Decision
55 days
Submission Type
Summary