Last synced on 14 November 2025 at 11:06 pm

ORTRAUTEK TRAUMA SYSTEM

Page Type
Cleared 510(K)
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)
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