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ORATEC INTERVENTIONS MODEL ORASTAT MONOPOLAR CAUTERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K973158
510(k) Type
Traditional
Applicant
ORATEC INTERVENTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
75 days
Submission Type
Statement

ORATEC INTERVENTIONS MODEL ORASTAT MONOPOLAR CAUTERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K973158
510(k) Type
Traditional
Applicant
ORATEC INTERVENTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
75 days
Submission Type
Statement