Last synced on 18 April 2025 at 11:05 pm

ARTHROFLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K865066
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
117 days

ARTHROFLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K865066
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/1987
Days to Decision
117 days