AUTOBAHN Nailing System

K171108 · Globus Medical, Inc. · HSB · Dec 29, 2017 · Orthopedic

Device Facts

Record IDK171108
Device NameAUTOBAHN Nailing System
ApplicantGlobus Medical, Inc.
Product CodeHSB · Orthopedic
Decision DateDec 29, 2017
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 888.3020
Device ClassClass 2
AttributesTherapeutic, Pediatric

Intended Use

The AUTOBAHN™ Tibial Nail is indicated for stabilization of fractures in skeletally mature patients, specifically fractures of the proximal and distal tibial shaft, open and closed tibial shaft fractures, certain pre- and postisthmic fractures, non-unions, pseudarthrosis, corrective osteotomies, prophylactic nailing of impending pathological fractures, tumor resections, simple long bone fractures, severely comminuted, spiral, large oblique and segmental fractures, polytrauma and multiple fractures, reconstruction, following turnor resection and grafting, supracondylar fractures, and bone lengthening and shortening. The AUTOBAHN™ Trochanteric Nail is indicated for treatment of fractures in adults and adolescents (12-21 years of age) in which the growth plates have for the following indications: basal neck fractures, fixation of stable and unstable intertrochanteric, and subtrochanteric fractures, pathologic fractures (including prophylactic use) in both trochanteric and diaphyseal regions, combinations of pertrochanteric, basal neck fractures. Iong subtrochanteric fractures, turnor resections, from trauma, nonunions, malunions, and revision procedures. AUTOBAHN™ Antegrade/Retrograde Femoral Nails are indicated for long bone fracture fixation in skeletally mature patients, specifically femoral fracture fixation, which may include the following: open and closed femoral fractures, pseudoarthrosis and correction osteotomy, pathologic fractures, impending pathologic fractures, supracondylar fractures, including those with intra-articular extension, ipsilateral femultibia fractures proximal to a total knee arthroplasty, fractures distal to hip joint, nonunions and malunions, poly trauma patients, fractures in the morbidly obese, fractures involving osteopenic bone, compound and simple shaft fractures, proximal, metaphyseal, and distal shaft fractures, closed supracondylar fractures involving femoral condyles, comminuted fractures with bone loss, and periprosthetic fractures.

Device Story

Intramedullary nailing system for internal bone fixation; consists of nails and locking screws. Available in various lengths/diameters to match patient anatomy. Used by orthopedic surgeons in clinical/OR settings. Implants provide mechanical stabilization of long bone fractures; facilitate healing via rigid fixation. Benefits include restoration of bone alignment and support for complex fracture patterns (e.g., comminuted, segmental, periprosthetic).

Clinical Evidence

Bench testing only. Mechanical testing performed per ASTM F1264 including static and dynamic four-point and cantilever bending, static torsion, and cutout testing. Bacterial endotoxin testing (BET) performed per ANSI/AAMI ST-72:2011.

Technological Characteristics

Materials: Titanium alloy, cobalt chromium molybdenum alloy, titanium molybdenum alloy, and PEEK polymer inserts. Design: Intramedullary nails and locking screws. Testing standards: ASTM F1264 (mechanical), ANSI/AAMI ST-72:2011 (BET).

Indications for Use

Indicated for stabilization/fixation of tibial, trochanteric, and femoral fractures in skeletally mature patients (and adolescents 12-21 years with fused growth plates for trochanteric nails). Includes open/closed fractures, non-unions, malunions, pathological fractures, tumor resections, and revision procedures.

Regulatory Classification

Identification

An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logos of the U.S. Department of Health & Human Services and the U.S. Food & Drug Administration (FDA). The Department of Health & Human Services logo is on the left, and the FDA logo is on the right. The FDA logo is in blue and includes the acronym "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text. December 29, 2017 Globus Medical Inc. Kelly Baker Senior Vice President, Regulatory and Clinical Affairs 2560 General Armistead Avenue Audubon, Pennsylvania 19403 ## Re: K171108 Trade/Device Name: AUTOBAHN Nailing System Regulation Number: 21 CFR 888.3020 Regulation Name: Intramedullary Fixation Rod Regulatory Class: Class II Product Code: HSB, JDS, HWC Dated: November 6, 2017 Received: November 7, 2017 ## Dear Kelly Baker: 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 of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. {1}------------------------------------------------ Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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. For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, # Mark N. Melkerson -S Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement below. #### DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration ## Indications for Use 510(k) Number (if known) K171108 Device Name AUTOBAHN™ Nailing System #### Indications for Use (Describe) The AUTOBAHN™ Tibial Nail is indicated for stabilization of fractures in skeletally mature patients, specifically fractures of the proximal and distal tibial shaft, open and closed tibial shaft fractures, certain pre- and postisthmic fractures, non-unions, pseudarthrosis, corrective osteotomies, prophylactic nailing of impending pathological fractures, tumor resections, simple long bone fractures, severely comminuted, spiral, large oblique and segmental fractures, polytrauma and multiple fractures, reconstruction, following turnor resection and grafting, supracondylar fractures, and bone lengthening and shortening. The AUTOBAHN™ Trochanteric Nail is indicated for treatment of fractures in adults and adolescents (12-21 years of age) in which the growth plates have for the following indications: basal neck fractures, fixation of stable and unstable intertrochanteric, and subtrochanteric fractures, pathologic fractures (including prophylactic use) in both trochanteric and diaphyseal regions, combinations of pertrochanteric, basal neck fractures. Iong subtrochanteric fractures, turnor resections, from trauma, nonunions, malunions, and revision procedures. AUTOBAHN™ Antegrade/Retrograde Femoral Nails are indicated for long bone fracture fixation in skeletally mature patients, specifically femoral fracture fixation, which may include the following: open and closed femoral fractures, pseudoarthrosis and correction osteotomy, pathologic fractures, impending pathologic fractures, supracondylar fractures, including those with intra-articular extension, ipsilateral femultibia fractures proximal to a total knee arthroplasty, fractures distal to hip joint, nonunions and malunions, poly trauma patients, fractures in the morbidly obese, fractures involving osteopenic bone, compound and simple shaft fractures, proximal, metaphyseal, and distal shaft fractures, closed supracondylar fractures involving femoral condyles, comminuted fractures with bone loss, and periprosthetic fractures. Type of Use (Select one or both, as applicable) 2 Prescription Use (Part 21 CFR 801 Subpart D) - Over-The-Counter Use (21 CFR 801 Subpart C) ### PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED. #### FOR FDA USE ONLY Concurrence of Center for Devices and Radiological Health (CDRH) (Signature) {3}------------------------------------------------ This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {4}------------------------------------------------ ## 510(k) Summary: AUTOBAHN™ Nailing System | Company: | Globus Medical Inc.<br>2560 General Armistead Ave.<br>Audubon, PA 19403<br>610-930-1800 | | |-----------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Contact: | Kelly J. Baker, Ph.D.<br>Senior Vice President, Regulatory and Clinical Affairs | | | Date Prepared: | December 20, 2017 | | | Device Name: | AUTOBAHN™ Nailing System | | | Common Name: | Intramedullary fixation rod<br>Single/multiple component metallic bone fixation appliances<br>and accessories<br>Smooth or threaded metallic bone fixation fastener | | | Classification: | Per 21 CFR as follows:<br>§888.3020 Intramedullary fixation rod<br>§888.3030 Single/multiple component metallic bone<br>fixation appliances and accessories<br>§888.3040 Smooth or threaded metallic bone fixation<br>fastener<br>Product Code: HSB, JDS, HWC<br>Regulatory Class: II, Panel Code: 87 | | | Predicates: | Nail | Predicate Device | | | Tibial | Synthes Tibial Nail System EX (K040762)*<br>T2 Tibial Nailing System (K131365)<br>TriGen® Meta-Nail Retrograde Femoral & Tibial<br>Nails (K061019)<br>Synthes Locking Screws (K000089) | | | Trochanteric | Gamma3® Nail System (K043431)*<br>Synthes Trochanteric Fixation Nail – Advanced<br>System (K131548) | | | A/R Femoral | Zimmer Natural Nail System Retrograde Femoral<br>Nails (K101622)*<br>Synthes Retrograde/Antegrade Femoral Nail<br>System (K033618)<br>Zimmer Natural Nail System Piriformis Fossa &<br>Greater Trochanter Antegrade Femoral Nails<br>(K083497)<br>T2 Femoral Nail (K112059) | Primary Predicates {5}------------------------------------------------ ## Purpose: The purpose of this submission is to request clearance for the AUTOBAHN™ Nailing System. ## Device Description: The AUTOBAHN™ Nailing System is a family of intramedullary nails and screws designed to be used for internal bone fixation. The implants are available in various lengths and diameters to accommodate a wide range of patient anatomy. The nails are secured with locking screws and all devices are manufactured from titanium alloy, cobalt chromium molybdenum alloy, or titanium molybdenum alloy, and may include radiolucent PEEK polymer inserts. ## Indications for Use: The AUTOBAHN™ Tibial Nail is indicated for stabilization of fractures in skeletally mature patients, specifically fractures of the proximal and distal tibia and the tibial shaft, open and closed tibial shaft fractures, certain pre- and postisthmic fractures, non-unions, malunions, pseudarthrosis, corrective osteotomies, prophylactic nailing of impending pathological fractures, tumor resections, simple long bone fractures, severely comminuted, spiral, large oblique and segmental fractures, polytrauma and multiple fractures, reconstruction, following tumor resection and grafting, supracondylar fractures, and bone lengthening and shortening. The AUTOBAHN™ Trochanteric Nail is indicated for treatment of fractures in adults and adolescents (12-21 years of age) in which the growth plates have fused for the following indications: basal neck fractures, fixation of stable and unstable intertrochanteric, pertrochanteric, and subtrochanteric fractures, pathologic fractures (including prophylactic use) in both trochanteric and diaphyseal regions, combinations of pertrochanteric, intertrochanteric, basal neck fractures, long subtrochanteric fractures, tumor resections, fractures resulting from trauma, nonunions, malunions, and revision procedures. AUTOBAHN™ Antegrade/Retrograde Femoral Nails are indicated for long bone fracture fixation in skeletally mature patients, specifically femoral fracture fixation, which may include the following: open and closed femoral fractures, pseudoarthrosis and correction osteotomy, pathologic fractures, impending pathologic fractures, tumor resections, supracondylar fractures, including those with intra-articular extension, ipsilateral hip/shaft fractures, ipsilateral femur/tibia fractures, fractures proximal to a total knee arthroplasty, fractures distal to hip joint, nonunions and malunions, poly trauma patients, fractures in the morbidly obese, fractures involving osteopenic and osteoporotic bone, compound and simple shaft fractures, proximal, metaphyseal, and distal shaft fractures, segmental fractures, closed supracondylar fractures involving femoral condyles, comminuted fractures, fractures with bone loss, and periprosthetic fractures. {6}------------------------------------------------ ## Performance Data: Performance of the AUTOBAHN™ Nailing System was evaluated in accordance with ASTM F1264. Engineering analysis and mechanical testing (static and dynamic four-point and cantilever bending, static torsion, and cutout) was performed for nails and screws. Performance data demonstrates substantial equivalence to the predicate devices. Bacterial endotoxin testing (BET) was conducted in accordance with ANSI/AAMI ST-72:2011. ## Technological Characteristics: The AUTOBAHN™ Nailing System implants have the same technological characteristics as the predicate devices including design, intended use, material composition, function, and range of sizes. ## Conclusions: The AUTOBAHN™ Nailing System has been found to be substantially equivalent to the predicate devices with respect to technical characteristics, performance, and intended use. The information provided within this premarket notification supports substantial equivalence to the predicate devices.
Innolitics
510(k) Summary
Decision Summary
Classification Order
Enter a record ID and click Load to view the document.
100%