Last synced on 18 April 2025 at 11:05 pm

Stabilynx PEEK Suture Anchor

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