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SPEEDLOCK KNOTLESS FIXATION DEVICE; 3.0MM DRILL; SHARP TIPPED OBTURATOR; LOW PROFILE DRILL GUIDDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111044
510(k) Type
Traditional
Applicant
ArthroCare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2011
Days to Decision
116 days
Submission Type
Summary

SPEEDLOCK KNOTLESS FIXATION DEVICE; 3.0MM DRILL; SHARP TIPPED OBTURATOR; LOW PROFILE DRILL GUIDDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111044
510(k) Type
Traditional
Applicant
ArthroCare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2011
Days to Decision
116 days
Submission Type
Summary