510(k) K242003

Device
XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
Applicant
Aesculap, Inc.
510(k) number
K242003
Product code
JXG
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-16
Date received
2024-07-09
Regulation
882.5550
Classification name
Shunt, Central Nervous System And Components
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Kathy Racosky
Address
3773 Corporate Pkwy. Center Valley PA US 18034 18034

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K233448Bactiseal EVD Catheter Sets; Bactiseal Clear EVD Catheter SetIntegra Lifesciences Production Corporation2023-12-19
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