510(k) K092538 · FTL Mesh, Surgical, Polymeric

REFINE SUPPORT SYSTEM, MODEL 100.0100

Applicant	Alure Medical, Inc., Santa Rosa CA, US
Decision	Substantially Equivalent, Mar 5, 2010
Received	Aug 19, 2009
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K092538

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.