← Product Code [LPH](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LPH) · K020170 # KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP (K020170) _Encore Orthopedics, Inc. · LPH · Feb 11, 2002 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LPH/K020170 ## Device Facts - **Applicant:** Encore Orthopedics, Inc. - **Product Code:** [LPH](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LPH.md) - **Decision Date:** Feb 11, 2002 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 888.3358 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use The Keystone® Hip System is intended for treatment of patients who are candidates for total hip arthroplasty because the natural femoral head and neck have been affected by osteoarthritis, inflammatory arthritis, traumatic arthritis, rheumatoid arthritis, avascular necrosis or femoral neck fracture, and revision arthroplasty. ## Device Story Keystone® Hip System is a cementless, semi-constrained, porous-coated hip prosthesis. System includes proximal bodies, distal stems, calcar replacement bodies, and modular calcar build-ups (+15mm, +30mm). Components connect via Morse-type taper junction with secondary fixation screw. Device used in total hip arthroplasty or revision surgery to address medial calcar bone deficiency; allows surgeon to rest stem calcar platform on remaining medial bone. Implanted by orthopedic surgeons in clinical/OR settings. Provides structural support for femoral reconstruction; benefits patients by restoring joint function and stability in cases of arthritis, necrosis, or fracture. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Materials: Wrought titanium-aluminum-vanadium alloy (Ti-6Al-4V) per ASTM F136. Porous coating per ASTM F1854-98. Design: Cementless, semi-constrained, porous-coated uncemented prosthesis. Modular assembly via Morse-type taper and attachment screws. Dimensions: Calcar build-ups available in +15mm and +30mm heights. ## Regulatory Identification A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement. ## Predicate Devices - Keystone® Hip System ([K000521](/device/K000521.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}------------------------------------------------ ## Summary of Safety and Effectiveness Encore Orthopedics®, Inc. 9800 Metric Blvd Austin, TX 78758 512-832-9500 ## FEB 1 1 2002 Trade Name: Keystone® Hip System Calcar Replacement Body and Build-up Common Name: Cementless hip stem Classification Name: Hip joint metal/polymer/metal semi-constrained porous coated uncemented prosthesis Description: The Keystone® Hip System is available in a variety of proximal bodies and distal stem diameter and length configurations. The proximal body and stem are attached via a Morse type taper junction with an axially loading screw providing secondary attachment. The bodies, stems, and fixation screws were cleared on 510(k) K000521. All components are manufactured from titanium alloy (Ti-6A1-4V) that conforms to ASTM F136 with a porous coating that conforms to ASTM 1854-98 applied to the proximal body. The additional components that are the subject of this Special 510(k) submission are the calcar replacement bodies and calcar build-ups. The calcar replacement bodies are to be used either with or without a calcar build-up. During revision surgery or treatment of intertrochanteric fractures, the medial calcar bone is often deficient. This implant allows the surgeon to rest the calcar platform of the stem on the remaining medial bone. The modular build-up is available in a +15 and +30mm height for each size stem. The build-up is attached to the stem using an attachment screw. The modular buildups are fabricated from wrought titanium-aluminum-vanadium alloy (Ti-6Al-4V) conforming to ASTM F136. The attachment screw is used to attach the calcar build-up to the calcar replacement bodies. The attachment screw is fabricated from wrought titanium-aluminum-vanadium alloy (Ti-6Al-4V) conforming to ASTM F136. Intended Use: The Keystone® Hip System is intended for treatment of patients who are candidates for total hip arthroplasty because the natural femoral head and neck have been affected by osteoarthritis, inflammatory arthritis, traumatic arthritis, rheumatoid arthritis, avascular necrosis or femoral neck fracture, and revision arthroplasty. Comparable Features to Predicate Device(s): Features comparable to predicate devices include same materials, design and indications. KOZO170 VI {1}------------------------------------------------ Image /page/1/Picture/1 description: The image is a seal for the Department of Health & Human Services - USA. The seal is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is an abstract image of a bird-like figure. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 FEB 1 1 2002 Ms. Joanna Droege Regulatory/QA Engineer Encore Medical Corporation 9800 Metric Boulevard Austin, Texas 78758 Re: K020170 Trade Name: Keystone® Hip System Calar Replacement Body and Build-up Regulation Number: 21 CFR 888.3358 Regulation Name: Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis Regulatory Class: Class II Product Code: LPH Dated: January 14, 2002 Received: January 17, 2002 Dear Ms. Droege: We have reviewed your Section 510(k) premarket 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) that do not require approval of a premarket approval application (PMA). You may, (Trefore, 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, oontons provisions or actice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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 or any I with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); 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. {2}------------------------------------------------ Page 2 - Ms. Joanna Droege This letter will allow you to begin marketing your device as described in your Section 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 21 CFR Part 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" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html. Sincerely yours, Miriam C. Provost for Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## 170 510(k) Number (if known): Keystone® Hip System Calcar Replacement Body and Build-up Device Name: __ Indications For Use: ## Keystone® Hip System Indications For Use The indications for use of the total hip replacement prosthesis include: noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis; theumatoid arthritis; correction of functional deformity; revision procedures where other treatments or devices have failed; and treatment of nonunion, femoral neck and trochanteric fractures of the proximal femur with head involvement, which is unmanageable using other techniques. This stem is to be pressfit. (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use _> (per 21 CFR 801.109) OR Over-The-Counter Use _________________________________________________________________________________________________________________________________________________________ (Optional Format 1-2-96)_ Muriam C. Provost (Division Sign-Off) Division of General, Restorative and Neurological Devices 510(k) Number_KO2_0170 OK II SKHS --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LPH/K020170](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LPH/K020170) **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. 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