Linear Reduction Clamp
Exposure. Reduction. Fixation.
Compressive reduction instrument to aid in long bone, pelvic, and acetabular fractures.
A versatile instrument set designed to aid in the reduction and ultimate fixation of fractures over a range of applications.
Modern Reduction.
Ratchet-based mechanism of action
Allows for consistent and repeatable compressive forces
Four hook options
Four different hook options with varying sizes and tip ends to suit your indication needs. Hook attachments can be oriented in eight different ways relative to the handle and can be changed intra-operatively.
Removable handle technology
The handle can be removed from the assembly without any loss of compressive forces. This allows for multiple hook attachments from the same set to be assembled and reduces obstruction at site-of-care.
Instrumentation made simple.
Cannulated compression rod for direct screw placement
Cannulated compression rod can accept ø2.7mm cortical, ø3.5mm cortical, ø4.5mm cortical, and ø6.5mm cancellous screws
Compatible with PRO system
Complements our existing PRO pelvis portfolio
Designed by surgeons, for surgeons.
Consistent
Compression
- Ratchet based mechanism of action allows for consistent and repeatable compressive forces
Enhanced
visibility and access
- Removable Handle allows for enhanced intraoperative visualization without loss of compression forces
- Four hook options of varying sizes and tip geometries to accommodate different applications and orientations
Direct
screw placement
- Cannulated compression rod for direct screw placement*
- Compatible with existing PRO pelvis portfolio
Linear Reduction Clamp resources
Discover more about the Linear Reduction Clamp by exploring our collection of clinical resources including surgery videos, brochures, and more.
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*Ø2.7mm cortical, Ø3.5mm cortical, Ø4.5mm cortical, and Ø6.5mm cancellous screws
This document is intended solely for the use of healthcare professionals. A surgeon must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that surgeons be trained in the use of any particular product before using it in surgery.
The information presented is intended to demonstrate a Stryker product. A surgeon must always refer to the package insert, product label and/or instructions for use, including the instructions for cleaning and sterilization (if applicable), before using any Stryker product. Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your Stryker representative if you have questions about the availability of Stryker products in your area.
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LRC-AWI-1, 02-2022