K243531
- 510(k) number
- K243531
- Device name
- Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology
- Applicant
- Integra Lifesciences Production Corporation MA · US
- Product code
- JXG — Shunt, Central Nervous System And Components
- Decision date
- 2025-08-08
- Date received
- 2024-11-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K243531.pdf
Official FDA record: K243531
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.