Last synced on 23 May 2025 at 11:06 pm

VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111983
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
129 days
Submission Type
Summary

VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111983
510(k) Type
Traditional
Applicant
ZIMMER TRABECULAR METAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2011
Days to Decision
129 days
Submission Type
Summary