# K043106: Pinn-Acl Crosspin

- Pathway: 510(k) (Traditional)
- Applicant: Linvatec Corp.
- Decided: Jan 19, 2005 after 71 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: 2 generations back to K933948 (1994). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011172: Arthrex Bio-Transfix, Arthrex, Inc. (2001) Summary page 2.
- K974341: Mitek BTB Absorbable (Pla) Cross Pin, Mitek Products (1998) Summary page 2.

## Indications for use
The Pinn-ACL® CrossPin is intended to provide femoral fixation of soft tissue grafts for reconstruction of cruciate ligaments in the knee.

Source page: https://510kreport.com/device/K043106
Methodology: https://510kreport.com/methodology