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VISTA -S DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070382
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2007
Days to Decision
111 days
Submission Type
Summary

VISTA -S DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070382
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2007
Days to Decision
111 days
Submission Type
Summary