Last synced on 14 November 2025 at 11:06 pm

MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM

Page Type
Cleared 510(K)
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)
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