# K121413: Crossfix II Memiscal Repair Device

- Pathway: 510(k) (Special)
- Applicant: Cayenne Medical, Inc.
- Decided: Jun 4, 2012 after 24 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K143356: NovoStitch Plus Meniscal Repair System (2015), 2 descendants of its own
- K180531: NovoStitch Pro Meniscal Repair System (2018), 1 descendant of its own
- K181772: NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0) (2018), 0 descendants of its own

## Indications for use
The CrossFix® 11 Meniscal Repair Device is intended for approximation of soft tissue in meniscal repair procedures.

Source page: https://510kreport.com/device/K121413
Methodology: https://510kreport.com/methodology