Synthes 202.832 2.7mm Cortex Screw Self-Tapping 32mm

Synthes 202.832 2.7mm Cortex Screw Self-Tapping 32mm

As a 2.7mm diameter screw with a 32mm length, it is a foundational component of the Synthes 2.7mm Mini-Fragment System. This screw is specifically designed for procedures where 3.5mm hardware is too large, but high pull-out resistance and significant reach are required for stabilizing fractures in the hand, foot, or distal radius.

Technical specifications

• Brand: Synthes
• Reference / model: 202.832
• Model: / REF: 202.832
• Material: 316L Stainless Steel (Surgical Grade)
• Diameter: 2.7 mm
• Overall Length: 32 mm

Additional product details

• Manufacturer: Synthes (DePuy Synthes)
• Thread Type: Self-Tapping / Fully Threaded
• Thread Pitch: 1.0 mm
• Core Diameter: 1.9 mm
• Head Diameter: 5.0 mm (Spherical)
• Drive Type: Small Hexagonal Socket
• Quantity: 1 Each
• Extended Bicortical Purchase: The 32mm length is ideal for spanning wider bone dimensions in the hand or foot, providing "two-point" bicortical fixation that is critical for resisting rotational and bending forces.
• Universal System Integration: The 5.0mm spherical head is designed to sit flush within Synthes 2.7mm DCP and LC-DCP plates.
• 316L Stainless Steel Biocompatibility: Forged from cold-worked surgical steel, the 202.832 is biologically inert and offers the high fatigue resistance necessary for early functional mobilization.
• Hand & Wrist Surgery: Fixation of metacarpal and carpal fractures or stabilization of corrective osteotomies.
• Foot & Ankle Surgery: Stabilization of metatarsal shaft fractures and small-fragment midfoot fusions.
• Pediatric Orthopedics: Precise fixation in pediatric long bone fractures where 3.5mm hardware may be anatomically contraindicated.
• Small Fragment Trauma: Supplemental fixation for fractures of the distal radius or lateral malleolus.
• Status: NEW — Factory Sealed.
• Integrity: This implant is securely housed within its original manufacturer's packaging. Both inner and outer seals are intact, ensuring full material integrity and suitability for clinical use in 2026.
• Sterilization Note: While provided in original packaging, this device is typically provided as a NON-STERILE implant. It MUST be properly cleaned and sterilized (standard steam autoclave) in accordance with validated hospital protocols and Synthes’ Instructions for Use (IFU) prior to clinical implantation.

Condition

New.