510(k) K111472 · LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

HELICON HIP SYSTEM, FEMORAL STEM, HELICON HIP SYSTEM, FEMORAL HEAD, COCR, HELICON HIP SYSTEM, ACETABULAR SHELL, HELICON

Applicant	Tgm Medical, El Dorado CA, US
Decision	Substantially Equivalent, Sep 6, 2011
Received	May 27, 2011
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K111472

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.