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VERASENSE Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150372
510(k) Type
Traditional
Applicant
Orthosensor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2016
Days to Decision
427 days
Submission Type
Summary

VERASENSE Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150372
510(k) Type
Traditional
Applicant
Orthosensor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/15/2016
Days to Decision
427 days
Submission Type
Summary