# K062863: Osteomed Extended 2.0/2.4CANNULATED Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Osteomed LP
- Decided: Oct 31, 2006 after 36 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 K013888 (2002). 5 ancestors in all.
310 later devices descend from it; 8 cite it directly.
0 of 316 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010783: 2.0/2.4 Cannulated Screw System, Osteomed Corp. (2001) Summary page 1.
- K954330: Super Screw 3.5 MM, Osteomed Corp. (1995) Summary page 1.
- K963433: Threaded Fixation Pin, Orthopaedic Biosystems, Ltd. (1996) Summary page 1.
- K031050: PCW Percutaneous Compression Wire, Millennium Medical Technologies, Inc. (2003) Summary page 1.

## Most influential descendants
- K103705: Low Profile Screws (2011), 219 descendants of its own
- K111253: Arthrex Distal Extremity Plate System (2011), 135 descendants of its own
- K112437: Arthrex Fracture System (2011), 91 descendants of its own
- K123241: Arthrex Fracture Plates (2013), 71 descendants of its own
- K111678: Ortho Solutions Extremity Fixation Implants for Osteosysnthesis (2012), 58 descendants of its own

## Indications for use
The Osteomed Extended 2.0/2.4 Cannulated Screw System is indicated for bone fixation of hand and foot following trauma or osteotomy. Screws and washers are intended for single use only.

Source page: https://510kreport.com/device/K062863
Methodology: https://510kreport.com/methodology