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ARTHROPHONOMETER

Page Type
Cleared 510(K)
510(k) Number
K862286
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1987
Days to Decision
205 days

ARTHROPHONOMETER

Page Type
Cleared 510(K)
510(k) Number
K862286
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1987
Days to Decision
205 days