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ARTHREX SUTURE ANCHOR SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K934327
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
742 days
Submission Type
Statement

ARTHREX SUTURE ANCHOR SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K934327
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1995
Days to Decision
742 days
Submission Type
Statement