510(k) K182082 · NEU Marker, Radiographic, Implantable

Tumark for Eviva, Tumark for Brevera

Applicant	Somatex Medical Technologies GmbH, Teltow, DE
Decision	Substantially Equivalent, Oct 31, 2018
Received	Aug 2, 2018
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K182082

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.