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VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133784
510(k) Type
Traditional
Applicant
Zimmer Trabecular Metal Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2014
Days to Decision
207 days
Submission Type
Summary

VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133784
510(k) Type
Traditional
Applicant
Zimmer Trabecular Metal Technology
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2014
Days to Decision
207 days
Submission Type
Summary