# K063719: Arthrex Crosspin, Model AR-1964P

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Mar 6, 2007 after 81 days
- Product code: HTY (Pin, Fixation, Smooth)
- 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: 1 generation back to K010633 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010633: Rigidfix Soft Tissue Acl Crosspin System, Mitek Products (2001) Summary page 1.

## Indications for use
The Arthrex CrossPinTM is intended to be used for tibial fixation of autograft or allograft ACL soft tissue grafts.

Source page: https://510kreport.com/device/K063719
Methodology: https://510kreport.com/methodology