APTUS TITANIUM OSTEOSYNTHESIS SYSTEM

K051567 · Medartis, Inc. · HRS · Aug 23, 2005 · Orthopedic

Device Facts

• Record ID: K051567
• Device Name: APTUS TITANIUM OSTEOSYNTHESIS SYSTEM
• Applicant: Medartis, Inc.
• Product Code: HRS · Orthopedic
• Decision Date: Aug 23, 2005
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 888.3030
• Device Class: Class 2
• Attributes: Therapeutic

Indications for Use

The APTUS® Titanium Fixation System is intended for use in hand and forearm fractures, osteotomies and arthrodeses.

Device Story

APTUS Titanium Fixation System consists of titanium implant plates and screws for internal fixation of small bones in hand and forearm. Plates available in various shapes (H-frame, straight, T, L) for specific anatomical segments. Screws include TriLock locking screws utilizing spherical three-point wedge locking design for locking plates, and conventional bone screws with double thread design, sharp thread profile, and tapering core diameter. Device used by surgeons in clinical settings to stabilize bone fractures, osteotomies, or arthrodeses. Surgeon selects appropriate plate/screw configuration based on fracture type and anatomical location. Fixation provides mechanical stability to bone segments, facilitating healing and restoring function.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Titanium bone fixation plates and screws. Locking mechanism: TriLock spherical three-point wedge. Conventional screws: double thread design, tapering core, atraumatic tip. Various plate geometries (H, straight, T, L).

Indications for Use

Indicated for hand and forearm fractures, osteotomies, and arthrodeses. Includes management of distal, middle, proximal phalangeal and metacarpal fractures (transversal, spiral, joint-involved, shaft, comminuted, dislocation, avulsion); DIP and PIP arthrodeses; and distal radius fractures (extra-articular/articular extension and flexion) and correction osteotomies via volar or dorsal approaches.

Regulatory Classification

Identification

Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

Predicate Devices

• Profyle™ Titanium Hand and Small Fragment System (K961497)
• Stryker® Leibinger Universal Distal Radius System (K040022)
• Distal Radius Fracture Repair System (K002775)
• Distal Radius Fracture Repair System (K023007)
• Distal Radius Fracture Repair System (K030198)
• Fragment Plate System (K041081)

Submission Summary (Full Text)

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510(k) Summary

# AUG 2 3 2005

Image /page/0/Picture/2 description: The image shows the text "K051567" in a handwritten-like font, followed by the text "APTUS® Titanium Fixation System" in a smaller, sans-serif font. The text appears to be part of a product label or document. The "APTUS®" portion includes a registered trademark symbol.

# 510(k) Summary APTUS® Titanium Fixation System, Medartis, Inc.

# ADMINISTRATIVE INFORMATION

| Manufacturer Name: | Medartis, Inc.<br>127 W Street Road, Suite 203<br>Kennett Square, PA 19348 |
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Telephone [phone] FAX [phone]

Kate Gehret

Official Contact:

Representative/Consultant:

Floyd G. Larson PaxMed International, LLC 11234 El Camino Real, Suite 200 San Diego, CA 92130 Telephone [phone] FAX [phone]

APTUS® Titanium Fixation System

DEVICE NAME

Common Name:

Classification Name:

· Single/multiple component metallic bone fixation appliances and accessories

Trade/Proprietary Name:

Plate, Fixation, Bone

### DEVICE CLASSIFICATION

FDA has classified bone fixation plates as Class II devices (21 CFR 888.3030). The product code for bonc fixation plates is HRS. This device classification is reviewed by the Orthopedic Devices Branch.

## INTENDED USE

The APTUS® Titanium Fixation System is intended for use in hand and forearm fractures, osteotomies and arthrodeses.

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#### 510(k) Summary

# DEVICE DESCRIPTION

The APTUS® Titanium Fixation System consists of implant plates and implant screws and is used for internal fixation of small bones.

#### APTUS Plates

Implant Modules are provided in sizes Hand 1.2, Hand 1.5, Hand 2.0, Hand 2.3 for miplant Modules are pro rised in oristius reconstruction plate system is used for fixation valious iniger segmonts. The distal for corrective osteotomies of the distal radius with of fractures or the under laccess. Variations of plate shapes include H frame, straight, T and L shaped.

#### APTUS Screws

Locking screws for the Radius and Hand 2.0 Lock product lines, designated TriLock™, utilize a spherical three point wedge locking design and are used with locking plates. Conventional bone screws have a double thread design and precisely cut sharp thread profile, tapering core diameter and atraumatic tip. The shorter screws have a small pitch in order to maintain optimal purchase in the bone, while the longer screws have a larger pitch in order to minimize the number of revolutions.

### EQUIVALENCE TO MARKETED PRODUCT

The APTUS® Titanium Fixation System is substantially equivalent in indications and design principles to the following predicate devices, each of which has been determined by FDA to be substantially equivalent to pre-amendment devices: Profyle™ Titanium Hand and Small Fragment System (K961497) from Howmedica (Stryker); Stryker® Leibinger Universal Distal Radius System (K040022) from Stryker Leibinger; and Distal Radius Fracture Repair System (K002775, K023007, K030198) and Fragment Plate System (K041081) from Hand Innovations.

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Image /page/2/Picture/1 description: The image shows the seal of the U.S. Department of Health and Human Services. The seal features a stylized eagle-like symbol with three curved lines representing wings or feathers. The symbol is positioned in the center of a circular border. The text "DEPARTMENT OF HEALTH AND HUMAN SERVICES, USA" is arranged around the border of the circle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

AUG 2 3 2005

Medartis, Inc. c/o Mr. Floyd G. Larson President PaxMed International, LLC 11234 El Camino Real, Suite 200 San Diego, California 92130

Re: K051567

Trade/Device Name: APTUS® Titanium System Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: II Product Code: HRS Dated: June 13, 2005 Received: June 14, 2005

Dear Mr. Larson:

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.

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 comply 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.

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Page 2 - Mr. Floyd G. Larson

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), please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Mark

Mark N. Melkerson Acting Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known): ____________________________________________________________________________________________________________________________________________________

Device Name: APTUS® Titanium Fixation System

Indications for Use:

The APTUS® Titanium Fixation System is intended for use in hand and forearm fractures, osteotomies and arthrodeses.

APTUS® Hand group:

- Management of the fractures of the distal, middle and proximal phalanges . and metacarpals
- Management of all types of transversal fractures, spiral fractures, fractures � near joints with or without joint involvement, shaft factures, comminuted fractures, dislocation fractures, avulsion fractures
- DIP and PIP arthrodoses t

APTUS® Radius 2.5 group:

- Management via radio volar approach of extra-articular extension and . flexion fractures, articular extension and flexion fractures, correction osteotomies for badly healed radius fractures
- Management via dorsal approach of rare extension fractures that cannot be . adequately reduced via volar approach, procedures for which the soft tissue conditions make a volar approach very difficult or impossible, correction osteotomies requiring stabilization from the dorsal side, carporadial fusions.

| | Prescription Use X<br>(Part 21 CFR 801 Subpart D) | AND/OR | Over-The-Counter Use ______<br>(21 CFR 801-Subpart C) |
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(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off)

| Page 1 of 1 | Division of General, Restorative, and Neurological Devices |
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| 510(k) Number | K051567 |
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