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LIMITED REUSE ARTHROSCOPIC BLADES

Page Type
Cleared 510(K)
510(k) Number
K955914
510(k) Type
Traditional
Applicant
Smith & Nephew Dyonics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1996
Days to Decision
55 days
Submission Type
Summary

LIMITED REUSE ARTHROSCOPIC BLADES

Page Type
Cleared 510(K)
510(k) Number
K955914
510(k) Type
Traditional
Applicant
Smith & Nephew Dyonics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1996
Days to Decision
55 days
Submission Type
Summary