ClearanceBrief
510(k) K011030 ยท JXG Shunt, Central Nervous System And Components

AESCULAP -MIETHKE SHUNT SYSTEM

ApplicantAesculap, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, Mar 1, 2002
ReceivedApr 5, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011030

DateFirm and productCodeLinked 510(k)
Dec 3, 2014Aesculap, Inc.
The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.
Terminated
JXGNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.