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AltiVate Reverse® Glenoid

Page Type
Cleared 510(K)
510(k) Number
K233481
510(k) Type
Traditional
Applicant
Encore Medical, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2024
Days to Decision
216 days
Submission Type
Summary

AltiVate Reverse® Glenoid

Page Type
Cleared 510(K)
510(k) Number
K233481
510(k) Type
Traditional
Applicant
Encore Medical, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2024
Days to Decision
216 days
Submission Type
Summary