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PREVENA RESTOR(TM) Incision Management System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181507
510(k) Type
Traditional
Applicant
KCI USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2019
Days to Decision
253 days
Submission Type
Summary

PREVENA RESTOR(TM) Incision Management System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181507
510(k) Type
Traditional
Applicant
KCI USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2019
Days to Decision
253 days
Submission Type
Summary