eCFR Reference Browser

---

title: "21 CFR §888.3660"

source: "https://www.ecfr.gov/current/title-21/section-888.3660"

title_number: "21"

volume_number: "8"

chapter_number: "Unknown"

subchapter_code: "H"

subchapter_subject: "MEDICAL DEVICES"

part_code: "888"

part_subject: "ORTHOPEDIC DEVICES"

subpart_code: "D"

subpart_subject: "Prosthetic Devices"

section_number: "888.3660"

section_subject: "Shoulder joint metal/polymer semi-constrained cemented prosthesis."

cfr_reference: "21 CFR 888.3660"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 800 to 1299"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

(a)Identification. A shoulder joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a shoulder 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 includes prostheses that have a humeral resurfacing component made of alloys, such as cobalt-chromium-molybdenum, and a glenoid resurfacing component made of ultra-high molecular weight polyethylene, and is limited to those prostheses intended for use with bone cement (§ 888.3027).

(b)Classification. Class II. The special controls for this device are:

(1)FDA's:

(i)“Use of International Standard ISO 10993 ‘Biological Evaluation of Medical Devices—Part I: Evaluation and Testing,’ ”

(ii)“510(k) Sterility Review Guidance of 2/12/90 (K90-1),”

(iii)“Guidance Document for Testing Orthopedic Implants with Modified Metallic Surfaces Apposing Bone or Bone Cement,”

(iv)“Guidance Document for the Preparation of Premarket Notification (510(k)) Application for Orthopedic Devices,” and

(v)“Guidance Document for Testing Non-articulating, ‘Mechanically Locked’ Modular Implant Components,”

(2)International Organization for Standardization's (ISO):

(i)ISO 5832-3:1996 “Implants for Surgery—Metallic Materials—Part 3: Wrought Titanium 6-aluminum 4-vandium Alloy,”

(ii)ISO 5832-4:1996 “Implants for Surgery—Metallic Materials—Part 4: Cobalt-chromium-molybdenum casting alloy,”

(iii)ISO 5832-12:1996 “Implants for Surgery—Metallic Materials—Part 12: Wrought Cobalt-chromium-molybdenum alloy,”

(iv)ISO 5833:1992 “Implants for Surgery—Acrylic Resin Cements,”

(v)ISO 5834-2:1998 “Implants for Surgery—Ultra-high Molecular Weight Polyethylene—Part 2: Moulded Forms,”

(vi)ISO 6018:1987 “Orthopaedic Implants—General Requirements for Marking, Packaging, and Labeling,” and

(vii)ISO 9001:1994 “Quality Systems—Model for Quality Assurance in Design/Development, Production, Installation, and Servicing,” and

(3)American Society for Testing and Materials':

(i)F 75-92 “Specification for Cast Cobalt-28 Chromium-6 Molybdenum Alloy for Surgical Implant Material,”

(ii)F 648-98 “Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants,”

(iii)F 799-96 “Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Forgings for Surgical Implants,”

(iv)F 1044-95 “Test Method for Shear Testing of Porous Metal Coatings,”

(v)F 1108-97 “Specification for Titanium-6 Aluminum-4 Vanadium Alloy Castings for Surgical Implants,”

(vi)F 1147-95 “Test Method for Tension Testing of Porous Metal,”

(vii)F 1378-97 “Standard Specification for Shoulder Prosthesis,” and

(viii)F 1537-94 “Specification for Wrought Cobalt-28 Chromium-6 Molybdenum Alloy for Surgical Implants.”

§888.3660 - Shoulder joint metal/polymer semi-constrained cemented prosthesis.