510(k) K083669 · DZE Implant, Endosseous, Root-Form

OBI

Applicant	Euroteknika, Montreal, Quebec, CA
Decision	Substantially Equivalent, Jun 8, 2009
Received	Dec 11, 2008
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K083669

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.