Synthes 281.34 145° DHS Plate-Standard Barrel 4 Holes/78mm

Synthes 281.34 145° DHS Plate-Standard Barrel 4 Holes/78mm

The Synthes 281.34 is a specialized implant within the Dynamic Hip Screw (DHS) System, specifically engineered for the stabilization of intertrochanteric, subtrochanteric, and basilar neck fractures. This 4-hole plate features a 145° neck-shaft angle and a standard-length barrel, offering a steep anatomical configuration for patients with high-angle femoral neck geometry.

Technical specifications

• Brand: Synthes
• Reference / model: 281.34
• Model: / REF: 281.34
• Material: 316L Surgical Stainless Steel
• Overall Length: 78 mm
• Angle: 145 degrees

Additional product details

• The DHS system is the biomechanical "gold standard" for internal hip fixation. It allows the femoral head fragment to slide along a lag screw (sold separately) within the plate's barrel.
• Manufacturer: Synthes (DePuy Synthes)
• Neck-Shaft Angle: 145° (Valgus Alignment)
• Barrel Type: Standard Barrel (38mm length)
• Hole Count: 4 Holes (DCP/LC-DCP profile)
• Screw Compatibility: 4.5mm Cortex Screws (shaft) / DHS Lag Screw (barrel)
• Quantity: 1 Each
• Dynamic Sliding Mechanism: The standard barrel is precision-honed to interface with the DHS lag screw. This allows for controlled postoperative shortening and impaction of the fracture, which is critical for stability in osteoporotic bone.
• 145° High-Angle Alignment: The 145° angle is specifically designed for patients with a more valgus proximal femoral anatomy.
• High-Fatigue 316L Stainless Steel: Forged from vacuum-melted surgical steel, this plate provides the structural rigidity needed to withstand cyclic loading during early 2026 mobilization protocols.
• Intertrochanteric Fractures: Stabilization of stable and unstable pertrochanteric fractures.
• Subtrochanteric Fractures: Providing a rigid lateral buttress when used with supplemental fixation.
• Valgus Osteotomies: Management of proximal femoral deformities requiring a high-angle correction.
• Status: NEW — Factory Sealed.
• Integrity: The implant is securely housed within its original manufacturer's packaging. Both inner and outer seals are intact, ensuring full material integrity and suitability for surgical use.
• Sterilization Note: This device is provided as a NON-STERILE implant. It MUST be properly cleaned and sterilized via validated steam autoclave protocols in accordance with facility guidelines and Synthes’ Instructions for Use (IFU) prior to clinical implantation.

Condition

New.