510(k) K093549 · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

44MM E1 ACETABULAR LINER WITH 44MM BIOLOX DELTA OPTION CERAMIC HEAD OR 44MM M A MAGNUM

Applicant	Biomet Manufacturing Corp, Warsaw IN, US
Decision	Substantially Equivalent, Dec 16, 2009
Received	Nov 17, 2009
Type	Special
FDA record	Open on fda.gov

Recalls that name K093549

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.