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ARTHREX ATRAUMATIC MINI-GRASPER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925455
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
115 days
Submission Type
Statement

ARTHREX ATRAUMATIC MINI-GRASPER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925455
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
115 days
Submission Type
Statement