Last synced on 18 April 2025 at 11:05 pm

POSTEROMEDIAL GUIDE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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