HOFFMANN II EXTERNAL FIXATION SYSTEM

K952730 · Howmedica Corp. · JEC · Sep 8, 1995 · Orthopedic

Device Facts

Record IDK952730
Device NameHOFFMANN II EXTERNAL FIXATION SYSTEM
ApplicantHowmedica Corp.
Product CodeJEC · Orthopedic
Decision DateSep 8, 1995
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 888.3040
Device ClassClass 2
AttributesTherapeutic

Indications for Use

This submission describes a system of external fixation components consisting of a Pin Clamp Assembly With Post, Pin Clamp Assembly without a Fixed Post, Rod-to-Rod Coupling, Pin-to-Rod Coupling, 30° Angled Post, Straight Post, Straight Aluminum Connecting Rod and Curved Aluminum or Stainless Steel Rods. These components are intended to be used in conjunction with Half Pins or Transfixing Pins of the Hoffmann® External Fixation System (reference K861766) for the stabilization of fractures of the tibia, femur, humerus, radius or pelvis.

Device Story

System of external fixation components including pin clamps, couplings, posts, and connecting rods; used to construct external frames for bone fracture stabilization. Components connect percutaneous pins to external rods to provide rigid stabilization. Used in clinical settings by surgeons; manual assembly of frame components at fracture site. Provides mechanical support to bone fragments during healing. Components manufactured from aluminum and stainless steel.

Clinical Evidence

Bench testing only. Static mechanical testing performed on Pin Clamp Assembly, Pin-to-Rod Coupling, and Rod-to-Rod Coupling. Components compared to original Hoffmann® components to verify equivalent mechanical performance.

Technological Characteristics

Components constructed from aluminum and stainless steel. System utilizes mechanical pin clamps, couplings, and rods to create an external frame. Manual assembly; no energy source or software. Sterilization method not specified.

Indications for Use

Indicated for stabilization of fractures of the tibia, femur, humerus, radius, or pelvis in patients requiring external fixation.

Regulatory Classification

Identification

A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.

Predicate Devices

Reference Devices

Submission Summary (Full Text)

{0} K952730 510(k) Summary SEP-8, 1995 Device: Hoffmann® II External Fixation System This submission describes a system of external fixation components consisting of a Pin Clamp Assembly With Post, Pin Clamp Assembly without a Fixed Post, Rod-to-Rod Coupling, Pin-to-Rod Coupling, 30° Angled Post, Straight Post, Straight Aluminum Connecting Rod and Curved Aluminum or Stainless Steel Rods. These components are intended to be used in conjunction with Half Pins or Transfixing Pins of the Hoffmann® External Fixation System (reference K861766) for the stabilization of fractures of the tibia, femur, humerus, radius or pelvis. Testing of the components of this System is presented in this document. Evaluations included static testing of the Pin Clamp Assembly, Pin-to-Rod Coupling and Rod-to-Rod Coupling. In each test set up, the Hoffmann® II component was compared to a comparable Original Hoffmann® component. Equivalency of this System is based on similarities in intended use, materials, design and operational principles to the Original Hoffmann® External Fixation System Components including the 5-Hole Ball Joint, 8x8 Articulating Coupling and 8x5 Articulating Coupling (Preamendment); Hoffmann® 5-Hole Lightweight Alloy Ball Joint ((K803166); Hex Fix™ External Fixation System (K841334); and Synthes External Fixator (Synthes). All of these devices are intended to be used in an external fixation frame to stabilize bone fragments. The Hoffmann® II External Fixation System components are manufactured from Aluminum and Stainless Steel. The Original Hoffmann® components named and the Synthes External Fixator are also manufactured from Stainless Steel. The Hoffmann® Lightweight Alloy Ball Joint is manufactured from Aluminum. The design of each of the components of the Hoffmann® II External Fixation System, as described in this submission, are equivalent to individual components of the named equivalent products. The basic operational principles for the construction and placement of the external fixation systems named, as well as the Hoffmann® II External Fixation System, are to provide external stabilization of a fracture by means of percutaneous pins connected to an external frame by means of Pin Clamps, Couplings and Rods. The method of site preparation and frame construction are similar for all devices named. Relative indications and contraindications for use are also the same. For information contact: Mary C. Spicer Manager, Regulatory Affairs Howmedica Inc. 359 Veterans Boulevard Rutherford, NJ 07070 (201) 507-7791 - Phone (201) 507-6870 - Fax 166 {1} DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service SEP - 8 1995 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20856 Ms. Mary C. Spicer Manager, Regulatory Affairs Howmedica, Inc. Pfizer Hospital Products Group 359 Veterans Boulevard Rutherford, New Jersey 07070-2584 Re: K952730 Trade Name: Hoffmann® II External Fixation System Regulatory Class: II Product Code: JEC Dated: June 14, 1995 Received: June 15, 1995 Dear Ms. Spicer: 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 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 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. 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 Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP 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. {2} Page 2 - Ms. Mary C. Spicer This letter will allow you to begin marketing your device as described in your 510(k) premarket notification immediately. An FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and permits your device to proceed to the market, but it does not mean that FDA approves your device. Therefore, you may not promote or in any way represent your device or its labeling as being approved by FDA. 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), promotion, or advertising please contact the Office of Compliance, Promotion and Advertising Policy Staff (HFZ-302) at (301) 594-4639. 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 at (301) 443-6597. Sincerely yours, Kimber C. Richter Kimber C. Richter, M.D. Acting Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health 2
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