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MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903620
510(k) Type
Traditional
Applicant
SMITH & NEPHEW DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1990
Days to Decision
66 days

MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903620
510(k) Type
Traditional
Applicant
SMITH & NEPHEW DYONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1990
Days to Decision
66 days