# K220839: Arthrex Compression FT Pins

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Sep 19, 2022 after 180 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K000684 (2000). 79 ancestors in all.
No later device cites it as a predicate yet.
0 of 80 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132217: Arthrex Compression FT Screws, Arthrex, Inc. (2013) Summary page 4.
- K182361: Arthrex Compression FT Screws, Arthrex, Inc. (2018) Summary page 4.

## Indications for use
The Arthrex Compression FT pins (1.9 mm) are intended for small bone fracture and osteotomy fixation in the hand, wrist, foot, ankle and knee. The Arthrex Compression FT pins (2.4 mm) are intended for fixation of small bone fragments, such as apical fragments, osteochondral fragments and cancellous fragments. Specific applications include the following: * Osteochondral fragments * Apical fragments (radial head, patellar rim, navicular, metacarpal/metatarsal) * Cancellous fragments * Carpal, metacarpal, and small hand bone » Tarsal and metatarsals * Phalanges » Intra-articular fractures » Ankle * Proximal and distal humerus » Proximal and distal radius * Proximal and distal ulna » Osteochondral fixation and fractures » Osteochondritis Dissecans » Fixation of fractures and osteotomies about the knee * Oblique fractures of the fibula * Reconstructive surgeries of the foot » Malleolar fixation

Source page: https://510kreport.com/device/K220839
Methodology: https://510kreport.com/methodology