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MODEL 9000 AT ANKLE CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K902707
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1990
Days to Decision
36 days

MODEL 9000 AT ANKLE CPM DEVICE

Page Type
Cleared 510(K)
510(k) Number
K902707
510(k) Type
Traditional
Applicant
SUTTER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1990
Days to Decision
36 days