Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4

K152171 · Orthofix Srl · KTT · Sep 28, 2015 · Orthopedic

Device Facts

• Record ID: K152171
• Device Name: Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4
• Applicant: Orthofix Srl
• Product Code: KTT · Orthopedic
• Decision Date: Sep 28, 2015
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 888.3030
• Device Class: Class 2
• Attributes: Therapeutic, Pediatric

Intended Use

The TL-HEX System is intended for limb lengthening by metaphyseal distractions, fixation of open and closed fractures, treatment of non-union or pseudoarthrosis of long bones and correction of bony or soft tissue defects or deformities. The TL-HEX System is intended for limb lengthening by metaphyseal distractions, fixation of open and closed fractures, treatment of non-union or pseudoarthrosis of long bones and correction of bony or soft tissue defects or deformities.

Device Story

Multilateral external fixation system; utilizes aluminum rings, double row footplates, adjustable struts, and stainless steel instrumentation (hex drivers, wrenches, pliers) with implantable half pins and wires. Used for limb lengthening, fracture fixation, and deformity correction. Includes web-based software to assist physicians in creating patient-specific strut adjustment schedules. Physician operates system in clinical setting; software output guides manual adjustment of six struts to achieve desired bone/tissue alignment. Benefits include precise, controlled correction of complex orthopedic conditions.

Clinical Evidence

No clinical data was needed to support safety and effectiveness. Bench testing only; software verification and validation performed per FDA guidance.

Technological Characteristics

Multilateral external fixation system. Materials: aluminum (rings, struts, clips), stainless steel (instrumentation). Components: rings, footplates, adjustable struts, half pins, wires. Connectivity: web-based software component. Software validation performed.

Indications for Use

Indicated for adults and pediatric subgroups (excluding newborns) for: post-traumatic joint contracture with loss of range of motion; fractures/disease causing joint contractures or loss of range of motion; fractures requiring distraction; open and closed fracture fixation; pseudoarthrosis of long bones; limb lengthening by epiphyseal or metaphyseal distraction; correction of bony or soft tissue deformities/defects; joint arthrodesis; and infected fractures or non-unions.

Regulatory Classification

Identification

Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

Predicate Devices

• Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.3 (K143125)

Submission Summary (Full Text)

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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

September 28, 2015

Orthofix Srl % Cheryl Wagoner Principal Consultant Wagoner Consulting LLC PO Box 15729 Wilmington, North Carolina 28408

Re: K152171

Trade/Device Name: Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4 Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: Class II Product Code: KTT, OSN Dated: July 31, 2015 Received: August 4, 2015

Dear Ms. Wagoner:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set

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forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours,

# Mark N. Melkerson -S

Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known) K152171

Device Name

Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4

Indications for Use (Describe)

The TL-HEX System is intended for limb lengthening by metaphyseal distractions, fixation of open and closed fractures, treatment of non-union or pseudoarthrosis of long bones and correction of bony or soft tissue defects or deformities. The TL-HEX System is intended for limb lengthening by metaphyseal distractions, fixation of open and closed fractures, treatment of non-union or pseudoarthrosis of long bones and correction of bony or soft tissue defects or deformities.

Indications, both for adults and all pediatric subgroups except newborns, include :

- Post-traumatic joint contracture which has resulted in loss of range of motion
· Fractures and disease which generally may result in joint contractures or loss of range of motion and fractures requiring distraction

- Open and closed fracture fixation
- · Pseudoarthrosis of long bones
- · Limb lengthening by epiphyseal or metaphyseal distraction
- · Correction of bony or soft tissue deformities
- · Correction of bony or soft tissue defects
- · Joint arthrodesis
- · Infected fractures or non-unions

| Type of Use (Select one or both, as applicable) | |
|------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------|
| <div> <span> <span style="font-size:16px">☑</span> Prescription Use (Part 21 CFR 801 Subpart D) </span> </div> | <div> <span> <span style="font-size:16px">☐</span> Over-The-Counter Use (21 CFR 801 Subpart C) </span> </div> |

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### 510(k) Summary (as required by 21 CFR 807.92)

| Submitter | Orthofix Srl |
|-----------|-------------------------------|
| | Via delle Nazioni, 9 |
| | 37012 Bussolengo (VR) - Italy |
| Telephone | + 39 045 6719.000 |
| Fax | + 39 045 6719.380 |

| Contact Person | Gianluca Ricadona<br>Quality & Regulatory Affairs Manager |
|----------------|-----------------------------------------------------------|
| Address | Via delle Nazioni, 9<br>37012 Bussolengo (VR) - Italy |
| Telephone | + 39 045 6719.000 |
| Fax | + 39 045 6719.380 |
| Email | [e-mail] |

September 28, 2015 Date Prepared

| Trade Name | Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.4 |
|---------------------|--------------------------------------------------------------------------------|
| Common Name | Multilateral Fixators and Accessories |
| Panel Code | Orthopaedic |
| Classification Name | Single/multiple component metallic bone fixation appliances and<br>accessories |
| Class | Class II |
| Regulation Number | 21 CFR 888.3030 |
| Product Code | KTT, OSN |

| Predicate Device | 510(k) # | Manufacturer |
|----------------------------------------------------------|----------|--------------|
| Orthofix TL-HEX True Lok<br>Hexapod System (TL-HEX) V1.3 | K143125 | Orthofix Srl |

| Description | The Subject device is a multilateral external fixation system. The System can<br>also be used with a web-based software component that is designed to be<br>used to assist the physician in creating a patient adjustment schedule that<br>assists in adjusting the six struts.<br><br>Components of the system include:<br>Full, 5/8 and 3/8 aluminum Rings Double Row Footplates Adjustable struts Aluminum strut clips (number and direction) Stainless steel instrumentation such as hex drivers, wrenches, and pliers Implantable components such as half pins and wires Web-based software |
|---------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Indications and<br>Intended Use | The TL-HEX System is intended for limb lengthening by metaphyseal or<br>epiphyseal distractions, fixation of open and closed fractures, treatment of<br>non-union or pseudoarthrosis of long bones and correction of bony or soft<br>tissue defects or deformities. The TL-HEX System is intended for limb<br>lengthening by metaphyseal or epiphyseal distractions, fixation of open and |

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| closed fractures, treatment of non-union or pseudoarthrosis of long bones<br>and correction of bony or soft tissue defects or deformities.<br>Indications, both for adults and all pediatric subgroups except newborns,<br>include:<br>• Post-traumatic joint contracture which has resulted in loss of range of<br>motion<br>• Fractures and disease which generally may result in joint contractures or<br>loss of range of motion and fractures requiring distraction<br>• Open and closed fracture fixation<br>• Pseudoarthrosis of long bones<br>• Limb lengthening by epiphyseal or metaphyseal distraction<br>• Correction of bony or soft tissue deformities<br>• Correction of bony or soft tissue defects<br>• Joint arthrodesis<br>• Infected fractures or non-unions | |
|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Technological<br>Characteristics<br>and Substantial<br>Equivalence | Documentation was provided to demonstrate that the Orthofix TL-HEX True<br>Lok Hexapod System (TL-HEX) V1.4 is substantially equivalent to the<br>predicate Orthofix TL-HEX True Lok Hexapod System (TL-HEX) V1.3 in<br>intended use, operating principle, basic design, materials and components. |
| Performance Data | The subject device hardware is identical to the predicate device so additional<br>testing of the hardware are not required. It was determined through risk<br>management that no new risks are introduced as a result of the modified<br>indication.<br><br>Software verification and validation testing was completed in conformance<br>with FDA's guidance document entitled “General Principles of Software<br>Validation; Final Guidance for Industry and FDA Staff." The results of<br>software testing indicate that the software performs as intended. The results<br>demonstrated that the Subject device presents no new worst case for<br>performance testing. The Subject device was therefore found to be<br>substantially equivalent to the predicate.<br><br>Clinical data was not needed to support the safety and effectiveness of the<br>Subject Device. |
| Conclusion | Based on the comparison to predicate device, the Subject Orthofix TL-HEX<br>True Lok Hexapod System (TL_HEX) V1.4 has been shown to be |