510(k) K053164 · HAW Neurological Stereotaxic Instrument

IPLAN FLOW

Applicant	Brainlab AG, Heimstetten, DE
Decision	Substantially Equivalent, Mar 23, 2006
Received	Nov 14, 2005
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K053164

No recall in the FDA data names this 510(k).

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