Last synced on 14 November 2025 at 11:06 pm

Maven Patient-Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K202019
510(k) Type
Traditional
Applicant
Paragon 28, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2021
Days to Decision
177 days
Submission Type
Summary

Maven Patient-Specific Instrumentation

Page Type
Cleared 510(K)
510(k) Number
K202019
510(k) Type
Traditional
Applicant
Paragon 28, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2021
Days to Decision
177 days
Submission Type
Summary