Last synced on 14 November 2025 at 11:06 pm

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology

Page Type
Cleared 510(K)
510(k) Number
K243531
510(k) Type
Traditional
Applicant
Integra Lifesciences Production Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2025
Days to Decision
267 days
Submission Type
Summary

Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology

Page Type
Cleared 510(K)
510(k) Number
K243531
510(k) Type
Traditional
Applicant
Integra Lifesciences Production Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2025
Days to Decision
267 days
Submission Type
Summary