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ActivOrtho Nitinol Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K181610
510(k) Type
Traditional
Applicant
ActivOrtho, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
266 days
Submission Type
Summary

ActivOrtho Nitinol Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K181610
510(k) Type
Traditional
Applicant
ActivOrtho, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
266 days
Submission Type
Summary