Kyphoplasty systems
5.5 X 24mm Citrefix XPress System
by Acuitive Technologies, Inc.
A bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that can be chemically degraded and typically absorbed via natural body processes (e.g., a copolymer, metal alloy).
Where to buy 5.5 X 24mm Citrefix XPress System
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5.5 X 24mm Citrefix XPress System models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 70-810-5524 | — | MR Safe | Available |
FDA clearances
- 510(k) K203334 February 2021
Procedures that use kyphoplasty systems
Frequently asked questions
What is 5.5 X 24mm Citrefix XPress System used for?
A bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that can be chemically degraded and typically absorbed via natural body processes (e.g., a copolymer, metal alloy).
Who makes 5.5 X 24mm Citrefix XPress System?
5.5 X 24mm Citrefix XPress System is made by Acuitive Technologies, Inc.. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does 5.5 X 24mm Citrefix XPress System come in?
The FDA device database does not list sizes for 5.5 X 24mm Citrefix XPress System. Check the instructions for use or ask a Acuitive Technologies, Inc. representative.
Is 5.5 X 24mm Citrefix XPress System MRI safe?
The FDA device database lists 5.5 X 24mm Citrefix XPress System as MR Safe. Always follow the specific MRI conditions in the labeling.
Is 5.5 X 24mm Citrefix XPress System FDA cleared?
5.5 X 24mm Citrefix XPress System is covered by FDA submission K203334.
How do I contact a Acuitive Technologies, Inc. sales representative?
Acuitive Technologies, Inc. has not listed representatives on LA Vascular yet. Visit the Acuitive Technologies, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.