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EMPOWR Revision VVC+ (Varus / Valgus Constrained), e+ Tibial Insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230169
510(k) Type
Traditional
Applicant
Encore Medical, L.P. dba Enovis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2023
Days to Decision
76 days
Submission Type
Summary

EMPOWR Revision VVC+ (Varus / Valgus Constrained), e+ Tibial Insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230169
510(k) Type
Traditional
Applicant
Encore Medical, L.P. dba Enovis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2023
Days to Decision
76 days
Submission Type
Summary