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TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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