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POSTEROMEDIAL GUIDE

Page Type
Cleared 510(K)
510(k) Number
K901765
510(k) Type
Traditional
Applicant
SMITH & NEPHEW DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1990
Days to Decision
68 days

POSTEROMEDIAL GUIDE

Page Type
Cleared 510(K)
510(k) Number
K901765
510(k) Type
Traditional
Applicant
SMITH & NEPHEW DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1990
Days to Decision
68 days