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ARTHREX PUDDU OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K973812
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1998
Days to Decision
246 days
Submission Type
Summary

ARTHREX PUDDU OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K973812
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1998
Days to Decision
246 days
Submission Type
Summary