Product Description

The ISKD is a unique concept in limb reconstruction that has greatly improved the potential to lengthen limbs. The ISKD combines the advantages of intramedullary stabilization with the mechanics of external distraction in one device, offering the ability to lengthen up to 8 cm with a simple nailing technique.

Implanted after osteotomy, the ISKD lengthens gradually in response to normal movements of the limb. The ISKD is designed to distract when rotation occurs at the osteotomy site.Because the ISKD is completely internal, the potential risk of infection is reduced compared to lengthening procedures that require external pins or wires. In addition, there is no scarring from pins moving through the soft tissues.

The ISKD is designed to lengthen for a predetermined distance and then stop. A range of sizes are available to offer lengthening for most patients.

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Indication

The ISKD is indicated for limb lengthening of the tibia and femur and is used for:

  • Post-traumatic lengthening
  • Lengthening following acute shortening
  • Lengthening in cases of congenital shortening
  • As an alternative to closed shortening

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Surgeon Benefits
  • Lengthening with a simple nailing technique
  • Gradual callus distraction provides a natural lengthening process
  • Lengthening in cases of congenital shortening
  • Mechanical alignment and stability is maintained during lengthening and throughout consolidation

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Surgeon Support Materials
Brochures: * Protected PDF files: You will not be able to copy or print.
Videos:

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Clinical References:
  • The Intramedullary Skeletal Kinetic Distractor (ISKD): First Clinical Results of a New Intramedullary Nail for Lengthening of the Femur and Tibia. Full Text Article (PDF 5KB)
  • Improved comfort in lower limb lengthening with the intramedullary skeletal kinetic distractor . Principles and preliminary clinical experiences. Full Text Article (PDF 314KB)

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Patient Benefits
  • Internal device reduces psychological and social stress
  • Less painful than other lengthening methods
  • Minimal scarring
  • No risk of pin-tract infections
  • Hand held monitor allows patients to follow their lengthening process

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Patient Support Materials
Brochures:
Videos:

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Part Reference Numbers
Femoral Lengtheners
Catalog # ISKD Diameter (mm) Maximum Distraction (mm) Start Length (mm) Max. End Length (mm)
F12-255-305 12.5 50 255 305
F12-300-350 12.5 50 300 350
F12-345-395 12.5 50 345 395
F12-255-335 12.5 80 255 335
F12-300-380 12.5 80 300 380
F12-345-425 12.5 80 345 425

Tibial Lengtheners
Catalog # ISKD Diameter (mm) Maximum Distraction (mm) Start Length (mm) Max. End Length (mm)
T10-215-265 10.7 50 215 265
T10-255-305 10.7 50 255 305
T10-300-350 10.7 50 300 350
T10-255-335 10.7 80 255 335
T12-215-265 12.5 50 215 265
T12-245-295 12.5 50 245 295
T12-255-305 12.5 50 255 305
T12-300-350 12.5 50 300 350
T12-255-335 12.5 80 255 335
T12-300-380 12.5 80 300 380

Tibial & Femoral Locking Screws
Catalog # Shaft Diameter (mm) Shaft Length (mm) Thread Length (mm)
S4820NS 4.8 20 7
S4825NS 4.8 25 7
S4830NS 4.8 30 7
S4835NS 4.8 35 7
S4840NS 4.8 40 7
S4845NS 4.8 45 7
S4850NS 4.8 50 9
S4855NS 4.8 55 9
S4860NS 4.8 60 9
S4865NS 4.8 65 9
S4870NS 4.8 70 12
S4875NS 4.8 75 12

ISKD Instrument Tray Kit
Part No. Description Quantity
10012 3 mm Allen Wrench 1
10017 6 mm Allen Wrench 1
11005 4.8 mm Drill Stop 2
11021A Drill Bit, Colibrated, 180 mm, 4.8 mm 2
11027A Drill Bit, Colibrated, 280 mm, 4.8 mm 2
11030A Drill Bit, Colibrated, 180 mm, 4.0 mm 2
17350 3.5 mm Hexagonal T-Wrench 2
17351 Locking Screw Depth Gauge 1
17354 8 mm Straight Trocar 1
17355 6 mm T-Wrench w/U-Joint 1
17357 13 mm Spanner 1
17360 Screw Guide 3
17379 Nylon Screw, Guide Locking Screws 2
17391 Screw Adapter, Femur 1
17392 Sliding Hammer w/detachable swing arm 1
17410 Handel w/Bar, Locking Screw, Tibia 1
17420 Guide Bar, Tibia 1
17430 Locking Rod, Tibia 1
17440 Tibial Proximal Outrigger 1
17470 Pointed Awl 1
17491 Screw Adapter, Tibia 1
17510 Handle with Bar Locking Screw 1
17520 Bar, Guide, Part A 1
17525 Bar, Guide, Tibia Nail 1
17530 Locking Rod, Femoral Nail 1
17565 Guide, Drill, 8.014-8 mm diameter 3
36017 Allen Wrench, 4 mm Polyhedral 1
170035 Black Handle w/Bayonet fitting 1
450134 Steri-Tray, ISKD Instrument, Empty 1

Supplemental Equipment
Part No. Description
650179 Surgeon Manual/Software CD
FTM2000 ISKD Monitor

Tibial & Femoral Revision Locking Screws
Catalog No. Shaft Diameter (mm) Shaft Length (mm)
RS4020 4.0 20
RS4025 4.0 25
RS4030 4.0 30
RS4035 4.0 35
RS4040 4.0 40
RS4045 4.0 45
RS4050 4.0 50
RS4055 4.0 55
RS4060 4.0 60
RS4065 4.0 65
RS4070 4.0 70
RS4075 4.0 75
RS4820 4.8 20
RS4825 4.8 25
RS4830 4.8 30
RS4835 4.8 35
RS4840 4.8 40
RS4845 4.8 45
RS4850 4.8 50
RS4855 4.8 55
RS4860 4.8 60
RS4865 4.8 65
RS4870 4.8 70
RS4875 4.8 75

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Web Resources
  1. www.ISKD.com
  2. www.limblengthening.com
  3. www.limblength.com
  4. www.llrs.org

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Contraindications
  1. Cases in which there is an active infection or irregular bone diameter that would prevent the insertion the ISKD Internal Limb Lengthener.
  2. Cases in which the ISKD Internal Limb Lengthener would cross joint spaces or open epiphyseal growth plates such as in skeletally immature patients.
  3. Cases in which there is an obliterated medullary canal or other conditions that tend to retard healing such as blood supply limitations, peripheral vascular disease or evidence of inadequate vascularity.
  4. Patients with poor bone quality or metabolic bone disorders such as severe osteopenia, osteoporosis, osteomyelitis, poorly controlled diabetes mellitus, Paget's disease, etc.
  5. Patients with malignancy or tumor of the bone to be lengthened.
  6. Patients unwilling or incapable of following postoperative care instructions.
  7. Cases requiring the use of magnetic resonance imaging (i.e., MRI) while the ISKD Internal Limb Lengthener is implanted. Do not subject patients implanted with an ISKD Internal Limb Lengthener to MRI.
WARNINGS
  1. The ISKD Internal Limb Lengthener and Locking Screw assembly cannot withstand the stresses of full weight bearing. The patient should utilize external support and/or restrict activities until consolidation occurs.
  2. Use of the ISKD System in patients with cardiac pacemakers is not recommended due to the presence of the magnet sealed inside the ISKD Internal Limb Lengthener. It is possible that the limb implanted with an ISKD Lengthener could come in close proximity to the implanted pacemaker.
  3. Use of the ISKD System in patients with gross obesity is not recommended.
  4. The ISKD System may not be appropriate for patients with poly-trauma.
  5. Use of the ISKD System in patients with an active nonunion of the tibia or femur is not recommended.
  6. Smoking, chronic steroid use and the use of other anti-inflammatory drugs have been determined to affect bone healing and could potentially have an adverse effect on the bone regenerate during the lengthening process.
PRECAUTIONS
  1. Examine all ISKD System components carefully PRIOR TO USE to assure proper working condition. If you believe an ISKD System component to be faulty, damaged or suspect DO NOT USE.
  2. Once implanted, the ISKD Internal Limb Lengthener will not stop distracting until it reaches the length pre-determined by the surgeon. Refer to the appropriate Operative Technique for instructions regarding X-ray technique, limb measurement and proper ISKD implant selection.
  3. It is essential that proper operative technique be followed for ISKD implantation. Refer to the appropriate ISKD Operative Technique.

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