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TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD

Page Type
Cleared 510(K)
510(k) Number
K081348
510(k) Type
Traditional
Applicant
TRIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2008
Days to Decision
156 days
Submission Type
Summary

TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD

Page Type
Cleared 510(K)
510(k) Number
K081348
510(k) Type
Traditional
Applicant
TRIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2008
Days to Decision
156 days
Submission Type
Summary