Last synced on 23 May 2025 at 11:06 pm

ORTRAUTEK TRAUMA SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032520
510(k) Type
Traditional
Applicant
TEKKA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2003
Days to Decision
89 days
Submission Type
Summary

ORTRAUTEK TRAUMA SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032520
510(k) Type
Traditional
Applicant
TEKKA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/2003
Days to Decision
89 days
Submission Type
Summary