(449 days)
No
The device description and performance studies focus on the mechanical and material properties of the feeding tube, with no mention of AI or ML.
No.
The device is described as a feeding tube intended for the delivery of nutrition and/or medications, which are supportive functions rather than direct therapeutic actions to treat a disease or condition.
No
Explanation: The device is a feeding tube designed for delivering nutrition and/or medications, not for diagnosing medical conditions.
No
The device description clearly outlines a physical medical device (a feeding tube) made of polyether-urethane with specific physical features like sideports, flaps, and markings. The performance studies also focus on physical properties like tensile strength, leakage, and biocompatibility. There is no mention of software as a component or the primary function of the device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to perform tests on samples taken from the human body (like blood, urine, or tissue) to provide information about a person's health.
- Device Description and Intended Use: The description clearly states the device is a feeding tube intended to deliver nutrition and/or medications directly to the small bowel. It is a physical device used for direct intervention within the body, not for analyzing samples outside the body.
- Lack of IVD Characteristics: There is no mention of analyzing biological samples, performing tests, or providing diagnostic information based on laboratory analysis.
Therefore, the Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube is a therapeutic device, not an in vitro diagnostic device.
N/A
Intended Use / Indications for Use
The Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube is intended to provide short-term enteral access for delivery of nutrition and/or medications to the small bowel in patients older than 12 years old.
Product codes (comma separated list FDA assigned to the subject device)
KNT
Device Description
The Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube consists of a 14 Fr polyether-urethane tube manufactured with a length of 153 cm. It has 5 sideports on the distal end for the purpose of delivering nutrition and/or medication. The shaft of the Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube includes 26-28 flaps cut into the tubing over the distal 40 cm segment of the device. These flaps provide a means for the catheter to be advanced by the natural peristaltic action of the gastrointestinal tract. The most distal flap is placed at approximately 2 cm from the distal tip of the catheter. Markings are placed along the shaft of the Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube in 5 cm increments (labeled at 10 cm increments). The proximal end of the shaft is attached to a red feeding adapter marked with the text "ENTERAL FEED/MED." The Tiger 2 " Self-Advancing Nasal Jejunal Feeding Tube will be supplied sterile and is intended for one-time use.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
small bowel
Indicated Patient Age Range
patients older than 12 years old.
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)
- Tensile Strength Testing: shows that the subject device should not break or crack during proper clinical use. The results showed that the predetermined acceptance criteria were met.
- Liquid Leakage Testing: Testing shows that the subject device should not leak during proper clinical use. The results showed that the predetermined acceptance criteria were met.
- Misconnection Testing: Testing shows that the connector should not provide a secure connection when forcefully assembled to any surface of the components of and should easily disengage from each connector of every other application category specified in ISO 80369-1:2010 or should a connection engage, then greater that 75% of the infusate should leak from the misconnection between the connector and the reference connector. All test results are considered acceptable.
- Biocompatibility Testing: demonstrated that the subject device conforms to the biocompatibility requirements based on its intended use. Per ISO 10993-1 and FDA guidance, testing for cytotoxicity, sensitization, intracutaneous irritation, pyrogen, subchronic toxicity, subacute toxicity, and acute systemic toxicity demonstrated the biocompatibility of the subject devices. All test results are considered acceptable.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 876.5980 Gastrointestinal tube and accessories.
(a)
Identification. A gastrointestinal tube and accessories is a device that consists of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding of the alimentary tract. This device may incorporate an integral inflatable balloon for retention or hemostasis. This generic type of device includes the hemostatic bag, irrigation and aspiration catheter (gastric, colonic, etc.), rectal catheter, sterile infant gavage set, gastrointestinal string and tubes to locate internal bleeding, double lumen tube for intestinal decompression or intubation, feeding tube, gastroenterostomy tube, Levine tube, nasogastric tube, single lumen tube with mercury weight balloon for intestinal intubation or decompression, and gastro-urological irrigation tray (for gastrological use).(b)
Classification. (1) Class II (special controls). The barium enema retention catheter and tip with or without a bag that is a gastrointestinal tube and accessory or a gastronomy tube holder accessory is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I (general controls) for the dissolvable nasogastric feed tube guide for the nasogastric tube. The class I device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 876.9.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
May 18, 2017
Cook Incorporated Erum B. Nasir Regulatory Affairs Specialist 750 Daniels Way Bloomington, IN 47404
Re: K160509
Trade/Device Name: Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube Regulation Number: 21 CFR§ 876.5980 Regulation Name: Gastrointestinal Tube and Accessories Regulatory Class: II Product Code: KNT Dated: April 12, 2017 Received: April 13, 2017
Dear Erum B. Nasir:
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. However, you are responsible to determine that the medical devices you use as components in the kit have either been determined as substantially equivalent under the premarket notification process (Section 510(k) of the act), or were legally on the market prior to May 28, 1976, the enactment date of the Medical Device Amendments. Please note: If you purchase your device components in bulk (i.e., unfinished) and further process (e.g., sterilize) you must submit a new 510(k) before including these components in your kit/tray. 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
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.
1
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); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
Benjamin/R. Fisher -S
Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K160509
Device Name
Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube
Indications for Use (Describe)
The Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube is intended to provide short-term enteral access for delivery of nutrition and/or medications to the small bowel in patients older than 12 years old.
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
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Image /page/3/Picture/0 description: The image shows the logo for Cook Medical. The word "COOK" is in white, sans-serif font on a red background. Below the word "COOK" is the word "MEDICAL" in white, sans-serif font on a darker red background.
510(k) SUMMARY Tiger 2TM Self-Advancing Nasal Jejunal Feeding Tube 21 CFR §876.5980 Date Prepared: 11 May 2017
| Submitted By: | |
|---|---|
| Applicant: | Cook Incorporated |
| Contact: | Erum B. Nasir, MS |
| Applicant Address: | Cook Incorporated |
| 750 Daniels Way | |
| Bloomington, IN 47404 | |
| Contact Phone Number: | (812) 335-3575 x102607 |
| Contact Fax Number: | (812) 332-0281 |
| Device Information: | |
| Trade Name: | Tiger 2™ Self-Advancing Nasal Jejunal Feeding Tube |
| Common Name: | Tubes, Gastrointestinal (And Accessories) |
| Classification Name: | Gastrointestinal tube and accessories |
| Regulation: | 21 CFR §876.5980 |
| Product Code | KNT |
Predicate Device:
The Tiger 2™ Self-Advancing Nasal Jejunal Feeding Tube, subject of this submission, is substantially equivalent to the predicate device, the Wilson-Cook Nasal Jejunal Feeding Tubes and Nasal Jejunal Feeding Tube with Flaps, cleared under 510(k) number K043203.
Device Description:
The Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube consists of a 14 Fr polyether-urethane tube manufactured with a length of 153 cm. It has 5 sideports on the distal end for the purpose of delivering nutrition and/or medication. The shaft of the Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube includes 26-28 flaps cut into the tubing over the distal 40 cm segment of the device. These flaps provide a means for the catheter to be advanced by the natural peristaltic action of the gastrointestinal tract. The most distal flap is placed at approximately 2 cm from the distal tip of the catheter. Markings are placed along the shaft of the Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube in 5 cm increments (labeled at 10 cm increments). The proximal end of the shaft is attached to a red feeding adapter marked with the text "ENTERAL FEED/MED." The Tiger 2 " Self-Advancing Nasal Jejunal Feeding Tube will be supplied sterile and is intended for one-time use.
4
Image /page/4/Picture/0 description: The image features the logo for Cook Medical. The logo is set against a red background. The word "COOK" is displayed in large, white, sans-serif letters at the top. Below "COOK", the word "MEDICAL" is written in smaller, white, sans-serif letters on a slightly darker red rectangle.
COOK INCORPORATED 750 DANIELS WAY, P.O. BOX 489 BLOOMINGTON, IN 47402-0489 U.S.A. 812.339.2235 TOLL FREE: 800.457.4500 WWW.COOKMEDICAL.COM
Intended Use:
The Tiger 2 Self-Advancing Nasal Jejunal Feeding Tube is intended to provide short-term enteral access for delivery of nutrition and/or medications to the small bowel in patients older than 12 years old.
Comparison to Predicate Device:
It has been demonstrated that the Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube is comparable to the predicate device. The Tiger 2" Self-Advancing Nasal Jejunal Feeding Tube is identical in terms of intended use, principles of operation, and basic technological characteristics to the predicate device. The material of construction has been modified from polyvinyl chloride (PVC) of the predicate to polyether-urethane. An enteral feeding connector is also included in the device set. The safety and effectiveness of the modifications are supported by testing. A comparison between the predicate devices and the device subject of this submission is presented in Table 1.
| Table 1 Substantial Equivalence Comparison | ||
|---|---|---|
| PREDICATE DEVICE | SUBJECT DEVICE | |
| Wilson-Cook Nasal Jejunal | ||
| Feeding Tubes and Nasal Jejunal | ||
| Feeding Tube with Flaps | ||
| (K043203) | Tiger 2TM Self-Advancing Nasal | |
| Jejunal Feeding Tube | ||
| Regulation Number | 876.5980 | 876.5980 |
| Product Code | KNT | KNT |
| Classification | Gastrointestinal tube and | |
| accessories | Gastrointestinal tube and | |
| accessories | ||
| Intended Use | Used for short-term enteral access | |
| for delivery of nutrition and/or | ||
| medications to the small bowel. | Intended to provide short-term | |
| enteral access for delivery of | ||
| nutrition and/or medications to the | ||
| small bowel in patients older than | ||
| 12 years old. | ||
| Length | 153 cm | Identical |
| Diameter | 14 French | Identical |
| Mode of operation | Flaps allow catheter to be pulled | |
| into the small intestine by | ||
| peristalsis | Identical | |
| Catheter material | Polyvinyl chloride (PVC) | Polyether-Urethane |
| Barbed reduction | ||
| connector material | Polypropylene | Identical |
| Tiger 2 adapter | ||
| material | Polyvinyl chloride (PVC) | Identical |
| Feeding Connector | N/A | Cedic Enteral Distal End ENFit |
| Transition Connector (K140581) |
Table 1 Substantial Equivalence Comparison
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Image /page/5/Picture/0 description: The image shows the logo for Cook Medical. The logo consists of the word "COOK" in white, uppercase letters on a red background. Below the word "COOK" is the word "MEDICAL" in white, uppercase letters on a darker red background. The logo is simple and clean, with a focus on the company name.
| PREDICATE DEVICE | SUBJECT DEVICE | |
|---|---|---|
| Wilson-Cook Nasal Jejunal | ||
| Feeding Tubes and Nasal Jejunal | ||
| Feeding Tube with Flaps | ||
| (K043203) | Tiger 2TM Self-Advancing Nasal | |
| Jejunal Feeding Tube | ||
| Sterilization, SAL | ETO, 10-6 | Identical |
| Packaging | Tyvek peel-open pouch | Identical |
Test Data:
The following tests were performed to demonstrate that the Tiger 2™ Self-Advancing Nasal Jejunal Feeding Tube met applicable design and performance requirements and support a determination of substantial equivalence.
- Tensile Strength Testing shows that the subject device should not break or crack during 0 proper clinical use. The results showed that the predetermined acceptance criteria were met.
- Liquid Leakage Testing – Testing shows that the subject device should not leak during proper clinical use. The results showed that the predetermined acceptance criteria were met.
- . Misconnection Testing - Testing shows that the connector should not provide a secure connection when forcefully assembled to any surface of the components of and should easily disengage from each connector of every other application category specified in ISO 80369-1:2010 or should a connection engage, then greater that 75% of the infusate should leak from the misconnection between the connector and the reference connector. All test results are considered acceptable.
- Biocompatibility Testing demonstrated that the subject device conforms to the ● biocompatibility requirements based on its intended use. Per ISO 10993-1 and FDA guidance, testing for cytotoxicity, sensitization, intracutaneous irritation, pyrogen, subchronic toxicity, subacute toxicity, and acute systemic toxicity demonstrated the biocompatibility of the subject devices. All test results are considered acceptable.
The results of these tests showed that the subject device met the design input requirements based on the intended use, and support the conclusion that this device does not raise new questions of safety or effectiveness and support a determination of substantially equivalence to the predicate device.