(28 days)
No
The device description focuses on the mechanical components of a stent and delivery system, with no mention of software, algorithms, or data processing that would indicate AI/ML.
Yes
The device is indicated for "palliation of malignant neoplasms in the biliary tree," which is a form of medical treatment aimed at alleviating symptoms and improving the quality of life, rather than curing the disease. This falls under the definition of therapeutic use.
No
The device is a stent delivery system indicated for the palliation of malignant neoplasms in the biliary tree, which is a therapeutic purpose, not a diagnostic one.
No
The device description clearly details a physical medical device (stent, balloon catheter, introducer tube) and its components, with no mention of software as the primary or sole component.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information about a person's health. This testing is done outside of the body (in vitro).
- Device Description and Intended Use: The description clearly states that this device is a stent and a delivery system intended for use within the biliary tree to palliate malignant neoplasms. This is an implantable medical device used for a therapeutic purpose, not for diagnostic testing of specimens.
The device is used directly within the patient's body for treatment, which is the opposite of an in vitro diagnostic.
N/A
Intended Use / Indications for Use
The Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTA™ PRO .035" Delivery System is indicated for use in the palliation of malignant neoplasms in the biliary tree.
The Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTATM PRO .035" Delivery System is indicated for the palliation of malignant neoplasms in the biliary tree.
Product codes
78 FGE
Device Description
The PALMAZ GENESIS Transhepatic Biliary Stent is a balloon-expandable, laser cut stent made from 316L Stainless Steel tubing. The stent is sold mounted on a Cordis percutaneous transluminal angioplasty (PTA) balloon catheter. The stent is provided in nominal, unexpanded stent lengths from 19 to 79 mm. The stent is designed for expansion to diameters from 8 to 10 mm, depending on the diameter of the associated balloon upon which it is mounted.
The Cordis OPTA PRO PTA balloon catheter, formerly known as the OPTA LP PTA Balloon Catheter, is used as a delivery system for the PALMAZ GENESIS Transhepatic Biliary Stent. The delivery system utilizes an over-the-wire design and is a catheter with a distal DURALYN™ balloon and a proximal Y-connector. Two radiopaque marker bands aid in stent placement. The injectate lumen (marked "THRU") is used to inject contrast medium via hand injection, and to track the catheter over a guide wire. The inflation lumen (marked "BALLOON") is used to inflate and deflate the balloon. The nominal balloon size is printed on the Y-connector.
A metal introducer tube is included in the packaging.
The PALMAZ GENESIS Transhepatic Biliary stent on OPTA PRO .035" Delivery System is provided sterile (via ethylene oxide) and is intended for single use only.
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 safety and effectiveness of the Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTA™ PRO .035" Delivery System have been demonstrated via data collected from non-clinical design verification tests and analyses.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
K012090, K012056, K971448, K981407, K991028
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.
0
Page 1/2
SEP - 7 2001
Cordis Europa N.V., a Johnson & Johnson company
Attachment 1
Special 510(k) Premarket Notification
KO1259D
Summary of Safety and Effectiveness
| Submitter: | Bert Roossien
Manager Regulatory Affairs
Cordis Europa, N.V.
Oosteinde 8
NL-9301 LJ Roden
The Netherlands | |
|-----------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------|
| | Tel: +31 - (5050) 22321
Fax: +31 - (5050) 22456
e-mail: broossie@crdnl.jnj.com | |
| Contact person: | Chuck Ryan
Manager, Regulatory Affairs
Cordis Corporation
7 Powder Horn Drive
Warren, New Jersey 07059
USA
Tel: 908.412.7446
Fax: 908.412.3915
e-mail: cryan@crdus.jnj.com | |
| Date prepared | 09 August 2001. | |
| General provisions | Trade name: | Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent
on OPTA™ PRO .035" Delivery System. |
| | Common Name: | Biliary stent and accessories |
| | Classification Name: | 21 CFR 876.5010 Biliary Catheter and accessories. |
| Device Classification | Class II. | |
| Name of predicate device(s) | Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent (ref. K012090)Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on SLALOM .018 Delivery System (ref. K012056)Cordis OPTA ™ PRO (formerly known as OPTA LP) PTA Balloon Catheter (ref. K971448, K981407, K991028) | |
1
Special 510(k) Premarket Notification
KD12590
ಬ್ಗ ೭
| Cordis Europa N.V.,
| a Johnson & Johnson company | Special 510(k) Premarket Notification |
|---|---|
| Performance | |
| standards | Performance standards have not been established for this device by the FDA under |
| section 514 of the Food, Drug and Cosmetic Act. | |
| Device | |
| Description | The PALMAZ GENESIS Transhepatic Biliary Stent is a balloon-expandable, laser cut |
| stent made from 316L Stainless Steel tubing. The stent is sold mounted on a Cordis | |
| percutaneous transluminal angioplasty (PTA) balloon catheter. The stent is provided | |
| in nominal, unexpanded stent lengths from 19 to 79 mm. The stent is designed for | |
| expansion to diameters from 8 to 10 mm, depending on the diameter of the | |
| associated balloon upon which it is mounted. |
The Cordis OPTA PRO PTA balloon catheter, formerly known as the OPTA LP PTA
Balloon Catheter, is used as a delivery system for the PALMAZ GENESIS
Transhepatic Biliary Stent. The delivery system utilizes an over-the-wire design and
is a catheter with a distal DURALYN™ balloon and a proximal Y-connector. Two
radiopaque marker bands aid in stent placement. The injectate lumen (marked
"THRU") is used to inject contrast medium via hand injection, and to track the
catheter over a guide wire. The inflation lumen (marked "BALLOON") is used to
inflate and deflate the balloon. The nominal balloon size is printed on the Y-
connector.
A metal introducer tube is included in the packaging.
The PALMAZ GENESIS Transhepatic Biliary stent on OPTA PRO .035" Delivery
System is provided sterile (via ethylene oxide) and is intended for single use only. |
| Intended Use | The Cordis PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035"
Delivery System is indicated for use in the palliation of malignant neoplasms in the
biliary tree. |
| Performance
Data | The safety and effectiveness of the Cordis PALMAZ GENESIS Transhepatic Biliary
Stent on OPTA PRO .035" Delivery System have been demonstrated via data
collected from non-clinical design verification tests and analyses. |
| | A statement of substantial equivalence to another product is required by 21
CFR 807.87 and relates only to whether the present product can be marketed
without prior reclassification or clinical approval. The present submission is
therefore not related to the coverage of any patent and is not to be interpreted
as an admission or used as evidence in a patent infringement lawsuit. As the
commissioner of the FDA stated: "A determination of substantial equivalence
under the Fedral Food, Drug and Cosmetic Act releted to the fact that the
product can be lawfully marketed without pre-market approval or
reclassification. The determination is not intended to have any bearing
whatsoever on the resolution of patent infringement suits." 42 Federal Register
42, 50 et seq. (1977). |
2
DEPARTMENT OF HEALTH & HUMAN SERVICES
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 arrangement of the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA". Inside the circle is a stylized image of three human profiles facing right, with flowing lines above them that resemble a bird's wings. The logo is black and white.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
7 2001 SEP
Cordis Corporation Cordis Europa, N.V. c/o Mr. Charles J. Ryan, RAC Manager, Regulatory Affairs 7 Powder Horn Drive WARREN NJ 07059
K012590 Re:
Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTATM PRO .035" Delivery System Regulatory Class: II 21 CFR 876.5010 Product Code: 78 FGE Dated: August 9, 2001 Received: August 10, 2001
Dear Mr. Ryan:
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.
3
Page 2 - Mr. Charles J. Ryan, RAC
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 Of R rat 007), advertise (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.
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 you to begin marketing your device as described in your 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 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 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,
Philip Phillips
Statland, M.D., Ph.D. Bernard E. Director Office of Device Evaluation Center for Devices and Radiological Health
Enclosure .
4
Page 1 of 1
510(k) Number (if known): K012590
Device Name: Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTA™ PRO .035" Delivery System
FDA's Statement of the Indications For Use for device:
The Cordis PALMAZ® GENESIS™ Transhepatic Biliary Stent on OPTA™ PRO .035" Delivery System is indicated for the palliation of malignant neoplasms in the biliary tree.
Nancy C broglon
(Division Sign-Off)
Division of Reproductive, Abdominal,
and Radmiogical Devices 510(k) Number _
OR Prescription Use v (Per 21 CFR 801.109)
Over-The-Counter Use