# K102410: Matryx Interference Screw (5.0-6.5MM)

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Linvatec
- Decided: Dec 21, 2010 after 119 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: 8 generations back to K933738 (1994). 38 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032894: Osteo Acl Screw Model;237020T, 237025T, 237030T, 238020T, 238025T, 238030T, 239020T, 239025T, 239030T, 231020T, 231025T,, Linvatec Biomaterials, Inc. (2004) Summary page 1.
- K052080: Matryx Interference Screw, Linvatec Biomaterials, Inc. (2005) Summary page 1.
- K060830: Milagro Interference Screw, Depuy Mitek, A Johnson & Johnson Company (2006) Summary page 1.
- K071091: Modification to Bilok Screw, Biocomposites, Ltd. (2007) Summary page 2.

## Most influential descendants
- K120589: Milagro Interference Screws (2012), 1 descendant of its own
- K122869: Milagro Interference Screws (2012), 0 descendants of its own

## Indications for use
The Genesys Matryxtm is for attaching soft tissue to bone in orthopedic surgical procedures. Genesys Matryx TM is intended to be used for interference fixation of soft tissue (including ligaments or tendons) to bone, where the implant sizes offered are patient appropriate. The implant operates in conjunction with appropriate postoperative immobilization, throughout the healing period, to attach soft tissue to bone.

Source page: https://510kreport.com/device/K102410
Methodology: https://510kreport.com/methodology