Last synced on 14 November 2025 at 11:06 pm

GMK REVISION EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K123721
510(k) Type
Traditional
Applicant
MEDACTA INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2013
Days to Decision
234 days
Submission Type
Summary

GMK REVISION EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K123721
510(k) Type
Traditional
Applicant
MEDACTA INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2013
Days to Decision
234 days
Submission Type
Summary