Who is the manufacturer of NEWFIX EXTERNAL FIXATION SYSTEM?

Technologia Y Diseno Industrial, S.A DE C.V filed the 510(k) submission for NEWFIX EXTERNAL FIXATION SYSTEM (K101338).

What is the FDA product code for NEWFIX EXTERNAL FIXATION SYSTEM?

KTT. It is classified under 21 CFR 888.3030 as a Class 2 device in the Orthopedic panel.

What is the regulatory pathway for NEWFIX EXTERNAL FIXATION SYSTEM?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like NEWFIX EXTERNAL FIXATION SYSTEM?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

NEWFIX EXTERNAL FIXATION SYSTEM

K101338 · Technologia Y Diseno Industrial, S.A DE C.V · KTT · Mar 14, 2011 · Orthopedic

Device Facts

Record ID	K101338
Device Name	NEWFIX EXTERNAL FIXATION SYSTEM
Applicant	Technologia Y Diseno Industrial, S.A DE C.V
Product Code	KTT · Orthopedic
Decision Date	Mar 14, 2011
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 888.3030
Device Class	Class 2
Attributes	Therapeutic, Pediatric

Intended Use

The Newfix® External Fixation System, consisting of axial fixators and frame components, is indicated for stabilization of open and/or unstable fractures where soft tissue injury precludes the use of other fracture treatments such as IM rodding or casting. NEWFIX® External Fixation System is intended for the fixation and for temporary or extended stabilization in cases such as: open fractures, closed fractures, poly-trauma fractures, supplement in the stabilization of minimal fixations in intra and extra articular fractures.

Device Story

Modular external fixation system; components include clamps, distractors, pins, carbon fiber rods, stainless steel tubes. Used in orthopedic/trauma settings for fracture stabilization. Physician assembles frame constructs using clamps (rod-to-rod, pin-to-rod) and fixation pins (smooth or self-drilling/self-tapping with diamond tip). System provides temporary or extended stabilization for fractures where internal fixation or casting is contraindicated. Benefits include modularity, frame construction flexibility, and stabilization of complex fractures. Supplied non-sterile for single-patient use.

Clinical Evidence

Bench testing only. Testing included validation of locking mechanisms per ASTM F 1541 and engineering analysis comparing Newfix components to Orthofix predicate devices. Materials and mechanical performance were verified using force verification machines and torque wrenches.

Technological Characteristics

Modular system; materials: Carbon fiber, Stainless Steel 17-4PH (AISI 630), Stainless steel 304, 316LS, Titanium alloys, Aluminum 6061-T6. Components: clamps, distractors, pins, rods. Pins: smooth/self-drilling/self-tapping with diamond tip. Standards: ASTM F 1541 (External Skeletal Fixation Devices), ASTM E 4 (Force Verification). Non-sterile, single-use.

Indications for Use

Indicated for stabilization of open/unstable fractures in pediatric and adult patients where soft tissue injury precludes IM rodding or casting; includes open, closed, and poly-trauma fractures, and stabilization of intra/extra-articular fractures.

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 Modulsystem Dynamic Axial Fixation System (K831576, k955848)
Synthes ® External Fixation System (K961350, k011034, k090658)
Extrafix External fixation System by QFX Technologies (k091258)
Smith & Nephew External Fixation System (K994143)
Hoffmann II Compact External Fixation System (K971755)
Zimmer Wristore Distal Radius Fracture Fixator (k012294)
Tecnología y Diseño Industrial (TDI) Newfix Screw, Wire, and Fixation System (K101254)
Treu-Instrumente GmbH Bone Fixation Screws and Pins (K083912)

Related Devices

K232897 — Arthrex Small External Fixation System · Arthrex, Inc. · Oct 18, 2023
K141912 — AOS SMALL BONE EXTERNAL FIXATION, THREADED HALF PINS, AOS SMALL BONE EXTERNAL FIXATION, CARBON FIBER RODS, AOS SMALL BON · Advanced Orthopaedic Solutions, Inc. · Oct 29, 2014
K181528 — Austin Miller Large External Fixation System · Austin Miller Trauma, LLC · Feb 28, 2019
K140675 — EMERGE EXTERNAL FIXATION SYSTEM · Emerge Medical, Inc. · Jun 10, 2014
K170146 — Galaxy UNYCO System · Orthofix Srl · Oct 12, 2017

Submission Summary (Full Text)

{0}------------------------------------------------ Tecnología y Diseño Industrial. S.A.P.I. de C.V Newfix® External Fixation System k101338 510(k) Summary #### MAR 1 4 2011 SUMMARY OF SAFETY AND EFFECTIVENESS March 11, 2010 Trade Name: Newfix® External Fixation System Common Name: External Fixation System Applicant: Tecnología y Diseño Industrial, S.A.P.I. de C.V. José Adán Ortega Torres Operation Manager José Guadalupe Zuno 48 Col. Parque Industrial los Belenes Zapopan, Jalisco Mexico, C.P. 45101 Tel: +52 (33) 38 36 45 00 Ext. 2960 +52 (33) 36245132 Fax: +52 (33) 38 36 45 02 Classification Name: Single/multiple component metallic bone fixation appliances and accessories Classification Panel: Orthopedic All questions and/or comments concerning this document should be made to: Robert J. Bard, Esq. Managing Director HealthCare Technologies Consultants PO Box 506 South Lyon, MI 48178 Tel: 248-573-5040 Cell: 734-330-5990 email: rbard@reglaw.net {1}------------------------------------------------ K101138 Tecnología y Diseño Industrial, S.A..P.I. de C.V. Newfix® External Fixation System k101338 510(k) Summary #### 1.0 DEVICE SUMMARY The Tecnología y Diseño Industrial, S.A. de C.V. Newfix® External Fixation System consists of various components including fixators, clamps, bars, distractors, carbon fiber rod, and stainless steel rods for use in orthopedic and trauma treatments. #### 1.1 Classification Information ### Table SE1: Device Classification | Classification or descriptor | Name or designation | |------------------------------|--------------------------------------------------------------------------------| | Common Name | External Fixation System | | Device Trade Name | Newfix® External Fixation System | | Device Classification Name | Single/multiple component metallic bone fixation appliances and accessories | | Device Classification | Class II | | Reviewing Panel | Orthopedic | | Regulation Number | 21 CFR 880.3030 | | Product Code | KTT | #### 2.0 PREDICATE DEVICES The Newfix® External Fixation System is substantially equivalent to the following predicate products. # Table SE2: Predicate Products | Manufacturer and Product | Cleared Predicate Product | |---------------------------------------------------------------------------------|------------------------------| | Orthofix Modulsystem Dynamic Axial Fixation System | K831576, k955848 | | Synthes ® External Fixation System | K961350, k011034, k090658 | | Extrafix External fixation System by QFX Technologies | k091258 | | Smith & Nephew External Fixation System | K994143 | | Hoffmann II Compact External Fixation System | K971755 | | Zimmer Wristore Distal Radius Fracture Fixator | k012294 | | Tecnología y Diseño Industrial (TDI) Newfix Screw, Wire, and Fixation System | K101254 | | Treu-Instrumente GmbH Bone Fixation Screws and Pins | K083912 | {2}------------------------------------------------ 16101338 Tecnología y Diseño Industrial, S.A..P.I. de C.V. Newfix® External Fixation System k101338 510(k) Summary #### 3.0 INTENDED USE AND INDICATIONS FOR USE The Newfix® External Fixation System, consisting of axial fixators and frame components, is indicated for stabilization of open and/or unstable fractures where soft tissue injury precludes the use of other fracture treatments such as IM rodding or casting. NEWFIX® External Fixation System is intended for the fixation and for temporary or extended stabilization in cases such as: open fractures, closed fractures, poly-trauma fractures, supplement in the stabilization of minimal fixations in intra and extra articular fractures. #### 4.0 DEVICE DESCRIPTIONS - 4.1 The Newfix External Fixation System is a modular system that consists of various components including clamps, distractors, pins, carbon fiber rod, and stainless steel tubes for use in orthopedic and trauma treatment. - 4.2 The system is a modular design to provide options in frame construction, simplicity in frame components, and ease of use. The system is comprised of aluminum and stainless steel clamps (rod-to-rod and pin-to-rod), stainless steel fixation pins and stainless steel and carbon fiber connector rods. Pins include smooth and self drilling/self-tapping type threaded pin with diamond tip and cutting edges. - 4.3 The Newfix® External Fixation System is supplied non sterile and is intended for single patient use. None of the components of the Newfix System are reusable. The Newfix® External Fixation System includes instruments and accessory devices necessary for its use. {3}------------------------------------------------ Tecnologia y Diseño Industrial, S.A..P.I. de C.V. COMPARISON OF DEVICE UNDER REVIEW AND ITS PREDICATI 5.0 | Comparison Element | TDI Newfix® External Fixation System K101338 | Orthofix Modulsystem Dynamic Axial Fixation System K955848 | Synthes® External Fixation System K961350, k011034, k090658 | XtraFix (Extrafix) External fixation System k091258 | Comparison Element | Materials | Duration of Use | Reuse Capability | |-----------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------|----------------------|------------------| | Manufacturer | Tecnología y Diseño Industrial S.A.P.I. de C.V. | Orthofix | Synthes (USA) | ExtraOrtho (QFX Technologies) | TDI Newfix® External Fixation System K101338 | Carbon fiber Stainless Steel 17-4PH (AISI 630) Stainless steel 304 Titanium alloys Aluminum 6061-T6 Stainless steel 316LS | Greater than 30 days | Single use | | Indication for/ Intended Use | The Newfix® External Fixation System, consisting of axial fixators and frame components, is indicated for stabilization of open and/or unstable fractures where soft tissue injury precludes the use of other fracture treatments such as IM rodding or casting. NEWFIX® External Fixation System is intended for the fixation and for temporary or extended stabilization in cases such as: open fractures, closed fractures, poly-trauma fractures, supplement in the stabilization of minimal fixations in intra and extra articular fractures. | Orthofix Dynamic Axial Fixation System is a unilateral external fixation device, which is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation and other bone conditions amenable to treatment by use of the external fixation modality." | The Synthes (USA) External Fixation Systems (K961350, k011034, k090658) are intended for use in the construction of an external fixator frame for the treatment of pediatric and adult fractures. | The Extrafix External Fixation System (k091258) includes various elements designed to build a fixator construct. The system includes clamps, posts, bars, and fixation pins. The Extrafix External Fixation System is indicated for use in construction of an external fixation frame for treatment of long bone (foot, femur, and tibia) and pelvic fractures that require external fixation. Specifically, the system is intended for: o Temporary stabilization of open or closed acute fractures with soft tissue injuries; o Definitive stabilization of open or closed fractures where open or alternative closed treatment is undesirable or otherwise contraindicated; o Stabilization of fractures in the context of polytrauma; o Temporary or definitive stabilization of certain pelvic fractures or pelvic ring injuries; o Arthrodesis and osteotomies with associated soft tissue problems; o Stabilization of limbs after removal of total joint (knee and ankle) arthroplasty for infection or other failure; o Neutralization of fractures stabilized with limited internal fixation; o Stabilization of non-unions; and o Intraoperative temporary stabilization tool to assist with indirect reduction. | Orthofix Modulsystem Dynamic Axial Fixation System K955848 | Aluminum, stainless steel, titanium, and composite materials | Greater than 30 days | Single use | | Synthes®. External Fixation System K961350, k011034, k090658 | Clamps -Stainless steel and titanium alloy Dynamization Clip - Stainless steel Rod Attachment - Stainless steel and titanium alloy Rods - Carbon fiber reinforced epoxy (CFRE) Screws - stainless, titanium alloys | Greater than 30 days | Single use | | | | | | | XtraFix (Extrafix) External fixation System k091258 | Aluminum, stainless steel, titanium, and composite materials | Greater than 30 days | Single use | | | | | | 上101338 Page 4 of 6 {4}------------------------------------------------ Tecnologia y Diseño Industrial, S.A..P.I. de C.V. Page 5 of 6 {5}------------------------------------------------ -101336 Tecnología y Diseño Industrial, S.A..P.I. de C.V. Newfix® External Fixation System k101338 510(k) Summary #### 5.1 Performance Tests - 5.1.1 Performance tests were conducted to validate the locking mechanism of the Newfix External Fixation System against various components of the Orthofix predicate devices. # TDI Products tested: - · E0300104 Lateral Cylinder for Pins (Straight Clamp). - · E0600201 T-Shaped Clamp. - . E0600301 Angled Clamp. - E0600401 Ankle Clamp. I - · E0900104/5 RadioLucent Wrist Axial Fixator Clamp. # Predicate Devices tested: - · Orthofix ProCallus Fixator Straight Clamp - · Orthofix T-Shaped Clamp - Orthofix Ankle Clamp . - · Orthofix RadioLucent Wrist Fixator Clamp # Materials used: - · Ø6mm (0.236in) and Ø4mm (0.157in) series 316 stainless steel rods. - Ø6mm (0.236in) and Ø4mm (0.157in) series 316 stainless steel rods with . a hexagonal nut for torque tests. - . Socket Set Screws Flat Point ISO 4026 M8x1.25. # Measuring tools: - · TDI.QC.023 PTS Analog push pull gauge SKN-5 S/N3409090760 - · TDI.QC.027 Dial torque wrench 6178A S/N 0207801708 ### Referenced Standards - · ASTM F 1541 Standard Specification and Test Methods for External Skeletal Fixation Devices. - · ASTM E 4 Practices for Force Verification of Testing Machines #### 6.0 CONCLUSION - Interconnection testing per ASTM F 1541 and engineering analysis comparing lock 6.1 mechanisms demonstrated equivalence to predicates. - The Newfix External Fixation System is substantially equivalent to the identified predicate 6.2 systems based on the substantial equivalence of indication for use, design features, operating principles, performance tests and material of composition. {6}------------------------------------------------ Image /page/6/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle or bird-like figure with three curved lines representing its body and wings. The bird is positioned to the right of a circular arrangement of text that reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA". Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 Technologia y Diseño Industrial, S.A.P.I. de C.V. % Healthcare Technologies Consultants Mr. Robert Bard PO Box 506 South Lyon, Michigan 48178 MAR 1 4 2011 Re: K101338 Trade/Device Name: Newfix® External Fixation System Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: Class II Product Code: KTT Dated: February 25, 2011 Received: March 01, 2011 Dear Mr. Bard: 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. Iisting 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. {7}------------------------------------------------ Page 2 - Mr. Robert Bard 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 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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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 Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely vours. Alvy B. Benson Mark N. Melkerson Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {8}------------------------------------------------ # Indication for Use 510(k): k101338 Device Name: Newfix® External Fixation System The Newfix® External Fixation System, consisting of axial fixators and frame components, is indicated for stabilization of open and/or unstable fractures where soft tissue injury precludes the use of other fracture treatments such as IM rodding or casting. NEWFIX® External Fixation System is intended for the fixation and for temporary or extended stabilization in cases such as: open fractures, closed fractures, poly-trauma fractures, supplement in the stabilization of minimal fixations in intra and extra articular fractures. Prescription Use X (21 CFR Part 801 Subpart D) and/or Over the Counter Use (21 CFR Part 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE; CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) M. Melkerson (Division Sign-Off) Division of Surgical, Orthopedic, and Restorative Devices 510(k)_ Number K101338 510(k) Number