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Stabilynx PEEK Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K142643
510(k) Type
Traditional
Applicant
D3 DC, LLC /Stabilynx, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2014
Days to Decision
89 days
Submission Type
Summary

Stabilynx PEEK Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K142643
510(k) Type
Traditional
Applicant
D3 DC, LLC /Stabilynx, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2014
Days to Decision
89 days
Submission Type
Summary