← Product Code [JDQ](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDQ) · K982545 # BMP CABLE SYSTEM (K982545) _Biomet, Inc. · JDQ · Oct 19, 1998 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDQ/K982545 ## Device Facts - **Applicant:** Biomet, Inc. - **Product Code:** [JDQ](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDQ.md) - **Decision Date:** Oct 19, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3010 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The BMP™ Cable System is indicated for general orthopedic repairs. This includes such procedures as long bone fractures, bone grafting, reinforcement of bone and reattachment of the greater trochanter. ## Device Story System for internal bone fixation; components include cables, sleeves, trochanteric grips, and cable plates. Cables (7x7 construction, cobalt chrome or stainless steel) provide tension for bone stabilization. Trochanteric grips and plates (316 LVM stainless steel or Co-Cr-Mo) facilitate fracture reduction and reattachment. Used by orthopedic surgeons in clinical/surgical settings. Surgeon threads cables around bone or through plates/grips, tensioning with T-handle tensioner and securing with crimps or sleeves. One-piece plate/sleeve design minimizes micromotion. Output is mechanical stabilization of bone segments; aids healing of fractures and osteotomies; reduces risk of nonunion or displacement. ## Clinical Evidence No clinical data provided; substantial equivalence based on design, material, and functional comparison to legally marketed predicate devices. ## Technological Characteristics Materials: 316 LVM stainless steel, cobalt chrome, titanium. Construction: 7x7 wire bundle cables (1.6mm/2.0mm diameter). Components: Cable sleeves, trochanteric grips (medium/large), cable plates (110mm-310mm), supracondylar plates, lateral trochanteric plates. Mechanical fixation via crimping and tensioning. Instruments: Cable passers, crimper, T-handle tensioner, cutters, impactors. ## Regulatory Identification A bone fixation cerclage is a device intended to be implanted that is made of alloys, such as cobalt-chromium-molybdenum, and that consists of a metallic ribbon or flat sheet or a wire. The device is wrapped around the shaft of a long bone, anchored to the bone with wire or screws, and used in the fixation of fractures. ## Predicate Devices - Dall-Miles Cable System ([K971741](/device/K971741.md)) - Dall-Miles Trochanter Cable Grip System ([K934058](/device/K934058.md)) - Osteo-Clage Cable System ([K921480](/device/K921480.md)) - J-Fx Cerclage System ([K971682](/device/K971682.md)) - Epi-Union Plating System ([K974289](/device/K974289.md)) - Osteo-Anatomical bone Plates ([K972196](/device/K972196.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K982545 1 of 2 ## SUMMARY OF SAFETY AND EFFECTIVENESS SPONSOR: Biomet, Inc. Airport Industrial Park Warsaw, Indiana 46580 Contact Person: Julie K. Ryan PROPIETARY NAME: BMP™ Cable System COMMON OR USUAL NAME: Metallic Internal Fixation Devices Cerclage Cable System CLASSIFICATION NAME: Bone, fixation Cerclage 888.3010 Plate, Fixation, Bone 888.3030 DEVICE CLASSIFICATION: Class II DEVICE PRODUCT CODE: 87 JDQ INTENDED USE: The BMP™ Cable System is indicated for general orthopedic repairs. This includes such procedures as long bone fractures, bone grafting, reinforcement of bone and reattachment of the greater trochanter. DESCRIPTION OF DEVICE: The BMP™ Cable System consists of cables, cable sleeves, trochanteric grip, cable plates and cable templates. The system also includes lateral trochanteric plates and supercondylar plates. The cables and cable sleeves are made of either cobalt chrome or stainless steel. All cables are 7x7 construction. Seven individual wires form a bundle and seven bundles are combined to form each cable optimizing strength and flexibility. The cobalt chrome is available in 2.0mm and 1.6mm diameter cables to be used with titanium and cobalt chrome implants. The stainless steel cables are 2.0mm diameter and used with stainless steel implant and the BMP cable plates. Three sleeves are available: 2.0mm CoCr. 1.6mm CoCr and 2.0mm stainless steel. The trochanteric grips are cobalt chrome and are available in two sizes – medium and large. Each grip has two crimp locations and do not require additional sleeves. The holes on the tronchateric grip are full radius. The cable plates are available in five lengths from 110mm to 310mm. Each plate is a one piece plate and sleeve construction manufactures from 316 LVM stainless steel. The one-piece construction allows for the sleeves to be machined directly on each plate, thus eliminating micromotion between the plate and sleeves. Stainless steel cable and screws are used to attach these plates to bone. The system includes templates for the corresponding plate size. A smaller plate for use on the humerous is being planned. {1}------------------------------------------------ K982545 2 of 2 There are two specialty plates in the system. The supracondylar cable plate comes in two lengths, 165 mm and 241 mm. The plate is manufactured out of 316 LVM stainless steel. Stainless steel screws and cables are used to attach this plate to bone. The lateral trochanteric plate is a Co-Cr-Mo plate that is manufactured in one length -185 mm. It is attached to the bone with titanium screws and Co-Cr- Mo cable. Instruments for use with these devices include cable passers, crimper, standard trochanteric grip impactor, T- handle tensioner, cable cutters, trochanteric grip manipulator/impactor and sterilization case. POTENTIAL RISKS: The potential risks associated with this device are the same as with any other clerclage system. These include but not limited to: Nonunion or delayed union Bending or fracture of the implant Metal sensitivity or allergic reaction to foreign body Limb shortening due to compression of fracture bone Bone resorption Decrease in bone density due to stress shielding Pain, discomfort, or abnormal sensations due to the presence of the device Nerve damage due to surgical trauma Necrosis of bone SUBSTANTIAL EQUIVALENCE: The BMP™ Cable System is substantially equivalent to most cable/Cerclage system on the market in overall design and intended function. Predicate devices include: Dall-Miles Cable System by Howmedica (K971741) Dall-Miles Trochanter Cable Grip System by Howmedica (K934058) Osteo-Clage Cable System by Acumed, Inc. (K921480) J-Fx Cerclage System by Johnson and Johnson (K971682) Epi-Union Plating System by Howmedica (K974289) Osteo-Anatomical bone Plates by Oestonics Corp.(K972196) {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized human figure with three arms or lines extending from the head, resembling a bird in flight. The figure is enclosed within a circular border, with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" arranged around the circle. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 OCT 19 1998 Ms. Julie K. Ryan Requlatory Specialist Biomet, Inc. P.O. Box 587 46581-0587 Warsaw, Indiana Re: K982545 BMP™ Cable System Trade Name: Regulatory Class: II Product Codes: JDQ and HRS Dated: July 17, 1998 Received: July 21, 1998 Dear Ms. Ryan: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act of the Act. include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. {3}------------------------------------------------ Page 2 - Ms. Julie K. Ryan This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ Page | of | ## 510 (K) NUMBER IF KNOWN: DEVICE NAME: BMP CABLE SYSTEM Indications of Use: There are several items that make up this system. They will be listed separately with their intended use: Cable Implants: Femur and Tibial Fractures Prophylactic banding Trochanteric reattachment Olecranon fractures Patella fractures Ankle fractures Fixation of spiral fractures in conjunction with I/M nailing and screwing techniques. Sternum fixation after open chest surgery Stabilization of cortical onlay strut graft Trochanteric Grip: Reattachment of greater trochanter following osteomy for total hip or total hip Procedures or trochanteric advancement Cable Plates Fixation of femoral, tibial or humeral fractures near the site of an intramedullary implant Fixation of fractures where a combination of screws and cerclage cables would improve stabilization Supracondylar Cable Plate Distal femoral fractures Subtrochanteric fractures Lateral Trochanteric Plate Extended trochanteric osteomies Trochanteric fractures (PLEASE DO NOT WRITE BELOW THEIS LINE-CONTINUE ON ANOTHER PAGE (IF NENDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use X (Per 21 CFR 801.109) or Over-the-CounterUse (Optional Format 1-2-96) t (Divide Sign Off) neral Res 510(k) Number Image /page/4/Picture/22 description: The image shows the number 00003 in a bold, sans-serif font. The numbers are black against a white background. The numbers are evenly spaced and aligned horizontally. The image is clear and easy to read. --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDQ/K982545](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDQ/K982545) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com