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Arthrex SS VAL and VAL KreuLock™ Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K243195
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2025
Days to Decision
101 days
Submission Type
Summary

Arthrex SS VAL and VAL KreuLock™ Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K243195
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2025
Days to Decision
101 days
Submission Type
Summary