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KAPP CUSTOM ULNAR HEAD WRIST IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K033930
510(k) Type
Traditional
Applicant
KAPP SURGICAL INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2004
Days to Decision
223 days
Submission Type
Summary

KAPP CUSTOM ULNAR HEAD WRIST IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K033930
510(k) Type
Traditional
Applicant
KAPP SURGICAL INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2004
Days to Decision
223 days
Submission Type
Summary