Last synced on 25 January 2026 at 3:41 am

CITRESPLINE and CITRELOCK ACL Implants

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210239
510(k) Type
Special
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
26 days
Submission Type
Summary

CITRESPLINE and CITRELOCK ACL Implants

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210239
510(k) Type
Special
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
26 days
Submission Type
Summary