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DYNAFLEX

Page Type
Cleared 510(K)
510(k) Number
K121396
510(k) Type
Traditional
Applicant
DYNA FLEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2012
Days to Decision
97 days
Submission Type
Summary

DYNAFLEX

Page Type
Cleared 510(K)
510(k) Number
K121396
510(k) Type
Traditional
Applicant
DYNA FLEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2012
Days to Decision
97 days
Submission Type
Summary