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ARTHROCARE ARTHROSCOPIC ELETROSURGERY SYSTEM (MODEL 980)

Page Type
Cleared 510(K)
510(k) Number
K963123
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1996
Days to Decision
57 days
Submission Type
Summary

ARTHROCARE ARTHROSCOPIC ELETROSURGERY SYSTEM (MODEL 980)

Page Type
Cleared 510(K)
510(k) Number
K963123
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1996
Days to Decision
57 days
Submission Type
Summary