K242003
- 510(k) number
- K242003
- Device name
- XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
- Applicant
- Aesculap, Inc. PA · US
- Product code
- JXG — Shunt, Central Nervous System And Components
- Decision date
- 2024-12-16
- Date received
- 2024-07-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242003.pdf
Official FDA record: K242003
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.