510(k) K221468

Device
Citregen? Tendon Interference Screw (TIS), Citrelock? Tendon Fixation Device, Citrespline? and Citrelock? ACL Implants
Applicant
Acuitive Technologies, Inc.
510(k) number
K221468
Product code
MAI
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-14
Date received
2022-05-20
Regulation
888.3030
Classification name
Fastener, Fixation, Biodegradable, Soft Tissue
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Matthew Poggie
Address
50 Commerce Dr. Alendale NJ US 07401 07401

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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