# K061620: Ifs Cannulated Bone Screw

- Pathway: 510(k) (Traditional)
- Applicant: Internal Fixation Systems, Inc.
- Decided: Jul 26, 2006 after 47 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: 2 generations back to K991151 (1999). 7 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050754: Precimed Cannulated Screw System, Precimed, Inc. (2005) Summary page 1.
- K053394: Nexa Bone Screw System, Nexa Orthopedics, Inc. (2005) Summary page 1.
- K990776: Aap Cannulated Screw, 7.5MM, 4.5MM, 4.0MM, 3.5MM, 7.0MM, Aap Implantate AG (1999) Summary page 1.
- K042310: Ortho-Pro Cannulated Bone Screws, Ortho-Pro, LLC (2004) Summary page 1.
- K991151: Vilex Cannulated Bone Screw, Duval Cannulated Bone Screw, Orthex Cannulated Bone Screw, Vilex, Inc. (1999) Summary page 1.
- K991197: Vilex/Duval/Orthex Cannulated Bone Screw, Models P222-XX, S25-XX, P227-XX, S30-XX, P235-XX, S35-XX, P240-XX, S40-XX, P24, Vilex, Inc. (1999) Summary page 1.

## Most influential descendants
- K063589: Gso Bone Fixation Fasteners (2007), 4 descendants of its own
- K071035: Ifs Bone Fixation Devices (2007), 3 descendants of its own
- K130613: Cannulated Screw and Kirschner (Kwire) System (2014), 1 descendant of its own
- K252758: Cannulated Screw and Kirschner (K wire) System (2025), 0 descendants of its own
- K140216: Orthopedic Fixation Systems (2014), 0 descendants of its own

## Indications for use
The Intended Use of the IFS Cannulated Bone Screw is for the treatment of bone fractures, such as fractures of the tarsals and metatarsals, and for metatarsals and phalangeal osteotomies and arthrodses of the hand and foot.

Source page: https://510kreport.com/device/K061620
Methodology: https://510kreport.com/methodology