Last synced on 18 April 2025 at 11:05 pm

Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221468
510(k) Type
Traditional
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2023
Days to Decision
270 days
Submission Type
Summary

Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221468
510(k) Type
Traditional
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2023
Days to Decision
270 days
Submission Type
Summary