# K092082: Synergy Cannulated Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Synergy Surgical Technologies, LLC
- Decided: Oct 2, 2009 after 85 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K113084: Renovis Cannulated Screw System (2011), 0 descendants of its own

## Indications for use
The Synergy Cannulated Screw System is intended for long and small bone fracture fixation, including: fractures of the tarsals and metatarsals; metatarsal and phalangeal osteotomies; fractures of the carpals and metacarpals; carpal and metacarpal arthrodesis; small fragments of the hand and wrist; ligament fixation as appropriate; sacroiliac joint disruptions; fractures of the distal femur and proximal tibia; intracapsular fractures of the hip; ankle arthrodesis; and pelvis and acetabulum fractures. This system is not indicated for use in the spine.

Source page: https://510kreport.com/device/K092082
Methodology: https://510kreport.com/methodology