HI-TOQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, #1009659,1009659J, 1009660, 10096

K013833 · Guidant Corp. · DQX · Jan 16, 2002 · Cardiovascular

Device Facts

• Record ID: K013833
• Device Name: HI-TOQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, #1009659,1009659J, 1009660, 10096
• Applicant: Guidant Corp.
• Product Code: DQX · Cardiovascular
• Decision Date: Jan 16, 2002
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 870.1330
• Device Class: Class 2

Intended Use

To facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The wire is also intended to facilitate the placement of compatible stent devices during therapeutic intravascular procedures.

Device Story

Steerable guide wire; max diameter 0.0137"; lengths 175 cm, 190 cm, 300 cm. Distal segment features Hydrocoat hydrophilic coating to reduce friction; proximal core coated with PTFE. Available in straight shapeable or pre-shaped "J" configurations. Used by physicians in clinical settings to navigate vasculature and facilitate placement of balloon dilatation catheters and stents during PTCA/PTA procedures. DOC extendable in specific lengths. Device acts as a mechanical track for interventional tools; improves maneuverability within catheters; aids in successful delivery of therapeutic devices to target lesion sites.

Clinical Evidence

No clinical data. Evidence consists of in vitro bench testing and in vivo performance evaluations demonstrating that the device meets acceptance criteria and performs similarly to predicate devices.

Technological Characteristics

Catheter guide wire; max diameter 0.0137"; lengths 175, 190, 300 cm. Materials include metal core with distal Hydrocoat hydrophilic coating and proximal PTFE coating. Steerable design; straight or pre-shaped "J" tip configurations. DOC extendable. Mechanical device; no software or energy source.

Indications for Use

Indicated for patients undergoing percutaneous transluminal coronary angioplasty (PTCA), percutaneous transluminal angioplasty (PTA), or therapeutic intravascular procedures requiring placement of balloon dilatation catheters or compatible stent devices.

Regulatory Classification

Identification

A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.

Special Controls

*Classification.* Class II (special controls). The device, when it is a torque device that is manually operated, non-patient contacting, and intended to manipulate non-cerebral vascular guide wires, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 870.9.

Predicate Devices

• HI-TORQUE BALANCE MIDDLEWEIGHTTM Guide Wire with Hydrocoat Hydrophilic Coating (K973494)
• HI-TORQUE WHISPERTM MS Guide Wire with Hydrocoat Hydrophilic Coating (K002206)

Submission Summary (Full Text)

{0}------------------------------------------------

# JAN 1 6 2002

#### 510(k) SUMMARY

The 510(k) Summary is submitted in accordance with 21 CFR §807.92 and the requirements of the SMDA of 1990.

| 1. Submitter's Name: | Guidant Corporation<br>Vascular Intervention |
|--------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 2. Submitter's Address: | 26531 Ynez Road |
| 3. Telephone: | [phone] |
| 4. Fax: | [phone] |
| 5. Contact Person: | Jennifer Pae Riggs |
| 6. Date Prepared: | November 16, 2001 |
| 7. Device Trade Name: | HI-TORQUE BALANCE MIDDLEWEIGHTTM<br>UNIVERSAL Guide Wires with Hydrocoat<br>Hydrophilic Coating |
| 8. Device Common Name: | Guide Wire |
| 9. Device Classification Name: | Catheter Guide Wire (74DQX) |
| 10. Predicate Device: | HI-TORQUE BALANCE MIDDLEWEIGHTTM Guide<br>Wire with Hydrocoat Hydrophilic Coating (K973494)<br>HI-TORQUE WHISPERTM MS Guide Wire with<br>Hydrocoat Hydrophilic Coating (K002206) |

11. Device Description:

The HI-TORQUE BALANCE MIDDLEWEIGHT™ UNIVERSAL Guide Wire is a steerable guide wire available in a maximum diameter of 0.0137" and in lengths of 175 cm, 190 cm and 300 cm. The distal segment of the guide wire, up to the hypotube, is coated with hydrocoat to reduce friction for improved guide wire movement within the catheter. The distal tip is offered in a straight shapeable configuration and a pre-shaped "J" configuration. The proximal core has a maximum diameter of 0.0137". The proximal end of the guide wire is coated with PTFE, which reduces friction of the wire within a catheter. The BMW™ Universal Guide Wire is DOC® extendable in the 175 cm and 190 cm lengths.

#### 12. Intended Use:

To facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The wire is also intended to facilitate the placement of compatible stent devices during therapeutic intravascular procedures.

13. Technological Characteristics:

Comparisons of the new and predicate devices show that the technological characteristics such as product performance, design and intended use are substantially equivalent to the current marketed predicate devices.

{1}------------------------------------------------

14. Performance Data:

In vitro bench testing and in vivo performance evaluations demonstrated that the HI-TORQUE BALANCE MIDDLEWEIGHT™ UNIVERSAL Guide Wire met the acceptance criteria and performed similarly to the predicate devices. No new safety or effectiveness issues were raised during the testing program and therefore, the HI-TORQUE BALANCE MIDDLEWEIGHT™ UNIVERSAL Guide Wire may be considered substantially equivalent to the predicate devices.

{2}------------------------------------------------

Image /page/2/Picture/1 description: The image is a black and white logo for the U.S. Department of Health and Human Services. The logo consists of a circular border with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized symbol that resembles an eagle or a bird in flight, composed of three curved lines that converge to form the shape of a bird's head and wings.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

JAN 1 6 2002

Guidant Corporation 26531 Ynez Road Temecula, CA 92591-4628

Sr. Regulatory Affairs Coordinator

Ms. Jennifer Pae Riggs

Re: K013833

HI-TORQUE BALANCE MIDDLEWEIGHT™ UNIVERSAL Guide Wires with Hydrocoat Hydrophilic Coating Regulation Number: 870.1330 Regulation Name: catheter guide wire Regulatory Class: Class II Product Code: DQX Dated: November 16, 2001 Received: November 19, 2001

Dear Ms. Riggs:

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

{3}------------------------------------------------

### Page 2 - Ms. Jennifer Pae Riggs

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.

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 promated notificate 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 [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. 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 [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Dalle Tuth

ram Zuckerman, M.D. Acting Director Division of Cardiovascular and Respiratory Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{4}------------------------------------------------

## INDICATION FOR USE STATEMENT

# 510(k) Number (if known): _ KO/ 3833

HI-TORQUE BALANCE MIDDLEWEIGHT™ UNIVERSAL Device Names: Guide Wire with Hydrocoat Hydrophilic Coating

Indications To facilitate the placement of balloon dilatation catheters during for Use: percutaneous transluminal coronary angioplasty (PTCA), percutaneous transluminal angioplasty (PTA) and compatible stent devices during therapeutic intravascular procedures.

(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 (Optional Format 1-1-96)

Nalle Teh
Division of Cardiovascule & Respiratory Devices
510(k) No K013833