Last synced on 18 April 2025 at 11:05 pm

Javelot Ti Suture Anchor, Javelot Ti-D Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232725
510(k) Type
Traditional
Applicant
Suzhou Endophix Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
57 days
Submission Type
Summary

Javelot Ti Suture Anchor, Javelot Ti-D Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232725
510(k) Type
Traditional
Applicant
Suzhou Endophix Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
57 days
Submission Type
Summary