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ARTHREX RING CURETTE

Page Type
Cleared 510(K)
510(k) Number
K925458
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
127 days
Submission Type
Statement

ARTHREX RING CURETTE

Page Type
Cleared 510(K)
510(k) Number
K925458
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
127 days
Submission Type
Statement