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CITRESPLINE and CITRELOCK ACL Implants

Page Type
Cleared 510(K)
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)
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