Condylar Plate 95 Degree Specification

SKU: FS-123 Category:

Description

Condylar Plate 95 Degree is intended for temporary fixation, correction or stabilization of bones in the proximal and/or distal femur.
Condylar Plate 95 Degree Specification
Plates are made of 316L stainless steel and Titanium.
The Condylar Plate is available in 50 mm, 60 mm, 70 mm and 80 mm blade length. Number of holes in plate are 5, 6, 7, 8, 9, 10, 11, 12, 14, 16 and 18 holes.
The angle between blade and shaft is 95 Degree in Plate.
Two first holes in plates next to blade used for 6.5 mm Cancellous Screw and rest holes in plates used for 4.5 mm Cortical Screws.
6.5 mm Cancellous Screws available thread lengths are 16 mm thread, 32 mm thread and Fully threaded. Screws are available in a wide range of length with 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115 and 120. Any extra Screws length will be made on order.
4.5 mm Cortical Screws are available in a wide range of length with 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 55, 60, 65, 70, 75, 80, 85 and 90mm. Any extra Screws length will be made on order.
The number of screw holes per plate length is maximized, without compromising plate strength. This allows an increased number of fixation points with a smaller incision.
General Instruments are available for Condylar Plate such as Plate Bending Press, Plate Holding Forceps, Plate Bending Pliers, Bone Holding Forceps, Bone Elevators, Bone Cutter, Bone Nibbler, Depth Gauge, Sleeve, Screw Driver, Trocar Sleeve etc.
Condylar Plate 95 Degree Uses
Condylar Plate is indicated for the fractures and revisions of the proximal and distal third of the femur in skeletally mature patients.
Condylar Plate Contraindications
Plate is contraindicated for use in areas with active or latent infection or insufficient quantity or quality of bone.
Precautions
Confirm functionality of instruments and check for wear during reprocessing. Replace worn or damaged instruments prior to use.
It is recommended to use the instruments identified for this plate.
Handle devices with care and dispose worn bone cutting instruments in a sharps container.
Always irrigate and apply suction for removal of debris potentially generated during implantation or removal.
Condylar Plate Warnings
Plate can break during use (when subjected to excessive forces). While the surgeon must make the final decision on removal of the broken part based on associated risk in doing so, we recommend that whenever possible and practical for the individual patient, the broken part should be removed. Be aware that implants are not as strong as native bone. Implants subjected to substantial loads may fail.
Instruments, screws and cut plates may have sharp edges or moving joints that may pinch or tear user’s glove or skin.
Take care to remove all fragments that are not fixated during the surgery.
While the surgeon must make the final decision on implant removal, we recommend that whenever possible and practical for the individual patient, fixation devices should be removed once their service as an aid to healing is accomplished. Implant removal should be followed by adequate post-operative management to avoid refracture.
General Adverse Events
As with all major surgical procedures, risks, side effects and adverse events can occur. While many possible reactions may occur, some of the most common include: Problems resulting from anesthesia and patient positioning (e.g. nausea, vomiting, dental injuries, neurological impairments, etc.), thrombosis, embolism, infection, nerve and/or tooth root damage or injury of other critical structures including blood vessels, excessive bleeding, damage to soft tissues incl. swelling, abnormal scar formation, functional impairment of the musculoskeletal system, pain, discomfort or abnormal sensation due to the presence of the device, allergy or hypersensitivity reactions, side effects associated with hardware prominence, loosening, bending, or breakage of the device, mal-union, non-union or delayed union which may lead to breakage of
the implant, reoperation.

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