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ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K933470
510(k) Type
Traditional
Applicant
KINETIX INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1994
Days to Decision
252 days
Submission Type
Summary

ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K933470
510(k) Type
Traditional
Applicant
KINETIX INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1994
Days to Decision
252 days
Submission Type
Summary