(29 days)
No
The provided text describes a mechanical stent and delivery system with no mention of AI or ML capabilities.
Yes
The device is a stent system intended for the "palliation of malignant neoplasms in the biliary tree," which describes a medical treatment for a disease.
No
This device is a stent system used for palliation of malignant neoplasms, meaning it is a therapeutic device designed to alleviate symptoms, not diagnose conditions.
No
The device description clearly outlines physical components such as a stent delivery system, stent material (Nickel Titanium alloy and tantalum micromarkers), expanded stent diameters and lengths, and a proximal deployment handle. This indicates it is a hardware device, not software-only.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is "palliation of malignant neoplasms in the biliary tree." This describes a therapeutic intervention (placing a stent to relieve obstruction), not a diagnostic test performed on samples outside the body.
- Device Description: The description details a physical implantable device (a stent) and its delivery system. This is characteristic of a medical device used for treatment, not a diagnostic reagent or instrument.
- Anatomical Site: The device is used within the "Biliary tree," which is an internal anatomical structure. IVDs typically analyze samples taken from the body (like blood, urine, tissue) in a laboratory setting.
An In Vitro Diagnostic (IVD) device is defined as a medical device that is used to perform tests on samples taken from the human body, such as blood, urine, or tissue, to provide information about a person's health. This device does not fit that description.
N/A
Intended Use / Indications for Use
The SMART™ Control™ Nitinol Stent Transhepatic Biliary System is intended for use in the palliation of malignant neoplasms in the biliary tree.
The Cordis S.M.A.R.T.™ Control™ Nitinol Stent Tranhepatic Biliary System is intended for use in the palliation of malignant neoplasms in the biliary tree.
Product codes
78 FGE
Device Description
The device description of the proposed SMART™ Control™ Nitinol Stent Transhepatic Biliary System is as follows.
• 6 French stent delivery system profile;
• Stent material - Nickel Titanium alloy and tantalum micromarkers;
• Expanded stent diameters 9 and 10 mm;
• Stent lengths: 80 mm;
• Stent delivery system usable length 80 and 120 cm; Guidewire lumen 0.035";
• Proximal Deployment Handle.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
biliary tree
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
The SMART™ Control™ Nitinol Stent Transhepatic Biliary System is substantially equivalent to the predicate devices. The equivalence was confirmed through pre-clinical testing.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 876.5010 Biliary catheter and accessories.
(a)
Identification. A biliary catheter and accessories is a tubular flexible device used for temporary or prolonged drainage of the biliary tract, for splinting of the bile duct during healing, or for preventing stricture of the bile duct. This generic type of device may include a bile collecting bag that is attached to the biliary catheter by a connector and fastened to the patient with a strap.(b)
Classification. Class II (special controls). The device, when it is a bile collecting bag or a surgical biliary catheter that does not include a balloon component, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.
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OCT 2 5 2002
510(k) Summary of Safety and Effectiveness
| General
| Provisions | The name of the device is: | |
|---|---|---|
| Proprietary Name | Common or Usual Name | |
| SMART™ Control™ Nitinol Stent | ||
| Transhepatic Biliary System | Biliary Stent | |
| Name of | ||
| Predicate | ||
| Devices | The device is substantially equivalent to: | |
| • Cordis SMART™ Control™ Nitinol Stent Transhepatic Biliary System | ||
| (510(k) # K021898 - August 14, 2001) - Cordis Corporation. | ||
| • S.M.A.R.T.™ Nitinol Stent and Delivery System (Improved Radiopacity) | ||
| (510(k) # K001843 – July 18, 2000 -- Cordis Corporation. | ||
| Classification | Class II. | |
| Performance | ||
| Standards | Performance standards have not been established by the FDA under section | |
| 514 of the Food, Drug and Cosmetic Act. | ||
| Indications | ||
| for Use | The SMART™ Control™ Nitinol Stent Transhepatic Biliary System is | |
| intended for use in the palliation of malignant neoplasms in the biliary tree. | ||
| Device | ||
| Description | The device description of the proposed SMART™ Control™ Nitinol Stent | |
| Transhepatic Biliary System is as follows. | ||
| • 6 French stent delivery system profile; | ||
| • Stent material - Nickel Titanium alloy and tantalum | ||
| micromarkers; | ||
| • Expanded stent diameters 9 and 10 mm; | ||
| • Stent lengths: 80 mm; | ||
| • Stent delivery system usable length 80 and 120 cm; Guidewire | ||
| lumen 0.035"; | ||
| • Proximal Deployment Handle. | ||
| Biocompatibility | All materials used in the SMART™ Control™ Nitinol Stent | |
| Transhepatic Biliary System are biocompatible. |
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The SMART™ Control™ Nitinol Stent Transhepatic Biliary System is Summary of Substantial substantially equivalent to the predicate devices. The equivalence was Equivalence confirmed through pre-clinical testing.
2
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of three overlapping human figures, possibly representing the department's focus on people and well-being.
OCT 2 5 2002
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. Sam Mirza Manager, Regulatory Affairs Cordis, a Johnson & Johnson Company 14201 N.W. 60th Avenue MIAMI LAKES FL 33014
Re: K023217
Trade/Device Name: Cordis S.M.A.R.T.TM Control™ Nitinol Stent Transhepatic Biliary System Regulation Number: 21 CFR 876.5010 Regulation Name: Biliary catheter and accessories Regulatory Class: II Product Code: 78 FGE Dated: September 25, 2002 Received: September 26, 2002
Dear Mr. Mr. Mirza:
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 (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). You may, therefore, market the device, subject to the general controls provisions of the Act and the limitations described below. 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.
The Office of Device Evaluation has determined that there is a reasonable likelihood that this device will be used for an intended use not identified in the proposed labeling and that such use could cause harm. Therefore, in accordance with Section 513(i)(1)(E) of the Act, the following limitation must appear in the Warnings section of the device's labeling:
The safety and effectiveness of this device for use in the vascular system have not been established.
Furthermore, the indication for biliary use must be prominently displayed in all labeling, including pouch, box, and carton labels, instructions for use, and other promotional materials, in close proximity to the trade name, of a similar point size, and in bold print.
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Page 2 - Mr. Sam Mirza
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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 (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
The 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. This letter will allow vou to begin marketing your device as described in your Section 510(k) premarket notification if the limitation statement above is added to your labeling, as described.
Please note that the above labeling limitations are required by Section 513(i)(1)(E) of the Act. Therefore, a new 510(k) is required before these limitations are modified in any way or removed from the device's labeling.
If you desire specific information about the application of other labeling requirements to your device (21 CFR Part 801 and additionally Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4616. 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"(21 CFR 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,
Daniel C. Schultz, M.
Daniel G. Schultz, M.D. Director Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Page 1 of 1
510(k) Number (if known): K023217
Device Name: Cordis S.M.A.R.T.TM Control™ Nitinol Stent Tranhepatic Biliary System
FDA's Statement of the Indications For Use for device:
The Cordis S.M.A.R.T.™ Control™ Nitinol Stent Tranhepatic Biliary System is intended for use in the palliation of malignant neoplasms in the biliary tree.
Prescription Use OR (Per 21 CFR 801.109)
Over-The-Counter Use__________________________________________________________________________________________________________________________________________________________
Urind A. Slymon