(28 days)
Not Found
No
The description focuses on the mechanical and material properties of a cannula for extracorporeal life support and does not mention any computational or analytical capabilities that would suggest AI/ML.
Yes
The device is used to drain and reinfuse blood during extracorporeal life support procedures, which is a therapeutic intervention to support failing organ function.
No
Explanation: The device is a cannula used for venous drainage and reinfusion of blood during extracorporeal life support; it facilitates treatment rather than providing diagnostic information.
No
The device description clearly outlines a physical, single-use cannula with specific material properties, design features (coaxial catheters, inflow openings), and sterilization methods. It is a hardware device intended for direct physical interaction with the patient's circulatory system.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for "venous drainage and reinfusion of blood via the internal jugular vein during extracorporeal life support procedures." This describes a therapeutic intervention involving the direct manipulation of blood within the body, not an in vitro test performed on a sample of blood or other bodily fluid outside the body.
- Device Description: The description details a cannula designed for insertion into a vein to facilitate blood flow in an extracorporeal circuit. This aligns with a medical device used for treatment or support, not for diagnostic testing.
- Lack of IVD Characteristics: There is no mention of the device being used to analyze blood or other samples, detect specific substances, or provide diagnostic information based on in vitro testing.
IVD devices are specifically designed to perform tests on samples taken from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. This device does not fit that description.
N/A
Intended Use / Indications for Use
The Quantum Perfusion Dual Lumen Cannula is intended for use as a single cannula for both venous drainage and reinfusion of blood via the internal jugular vein during extracorporeal life support procedures for periods of maximum 6 hours.
Product codes
DWF
Device Description
Quantum Perfusion Dual Lumen Cannula product family are single use devices intended to be used in medical procedures providing cardiac and/or respiratory support up to 6 hours. Devices are characterized by two coaxial catheters and are designed to be coupled with an extracorporeal circuit for artificial oxygenation of the blood and carbon dioxide removal.
Devices exploit a single site insertion which reduces the invasiveness of extracorporeal procedures. It can be inserted via a percutaneous approach through the right internal jugular vein. Blood is drained through the lumen of the outer catheter and returned through the lumen of the inner catheter.
Devices feature multiple inflow openings in the outer catheter limiting the circulation of unoxygenated blood.
Devices are non-toxic, non-pyrogenic, sterilized by ethylene oxide and packaged in a double pouch. All the devices' surfaces in contact with blood are coated with a phosphorylcholine-based biocompatible material.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
internal jugular vein
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)
NON-CLINICAL TESTING
The following activities were performed to demonstrate product safety and effectiveness, considering the proposed change and related impact:
- Update of labeling and Instructions for Use (IFU) according to ISO 15223-1:2021 Medical Devices - Symbols to Be Used with Medical Device Labels, Labelling, And Information to Be Supplied - Part 1: General Requirements [Recognition Nr. 5-134];
- Performance tests for new REF codes introduced in the portfolio, according to applicable Recognized Consensus Standard ISO 18193:2021 [Recognition Nr. 3-176].
Animal Study
No animal studies have been performed to support changes object of the present Special 510(k).
CLINICAL TESTING
No clinical data have been included in the current 510(k) submission to support substantial equivalence to legally marketed predicate devices.
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
§ 870.4210 Cardiopulmonary bypass vascular catheter, cannula, or tubing.
(a)
Identification. A cardiopulmonary bypass vascular catheter, cannula, or tubing is a device used in cardiopulmonary surgery to cannulate the vessels, perfuse the coronary arteries, and to interconnect the catheters and cannulas with an oxygenator. The device includes accessory bypass equipment.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which consists of the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG" in blue, and then the word "ADMINISTRATION" in a smaller font size below.
May 31, 2024
Spectrum Medical s.r.l. Raffaella Tommasini QA&RA Director via di Mezzo, 23 Mirandola, MO 41037 Italy
Re: K241248
Trade/Device Name: Quantum Perfusion Dual Lumen Cannula 31F-V1 Regulation Number: 21 CFR 870.4210 Regulation Name: Cardiopulmonary bypass vascular catheter, cannula, or tubing Regulatory Class: Class II Product Code: DWF Dated: May 3, 2024 Received: May 3, 2024
Dear Raffaella Tommasini:
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 (the 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.
Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).
1
Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30, Design controls; 21 CFR 820.90, Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review. the OS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).
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 of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Eric E. Richardson -S/A
for Nicole Gillette Assistant Director DHT2B: Division of Circulatory Support, Structural and Vascular Devices OHT2: Office of Cardiovascular Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
2
Indications for Use
510(k) Number (if known) K241248
Device Name
Quantum Perfusion Dual Lumen Cannula 31F-V1
Indications for Use (Describe)
The Quantum Perfusion Dual Lumen Cannula is intended for use as a single cannula for both venous drainage and reinfusion of blood via the internal jugular vein during extracorporeal life support procedures for periods of maximum 6 hours.
Type of Use (Select one or both, as applicable)
| Remediation Under Part 201, CERCLA, or Other | So That Corrective Action (s) CERCLA 35 |
|---|---|
| ---------------------------------------------- | ----------------------------------------- |
Prescription Use (Part 21 CFR 801 Subpart D)
| | Over-The-Counter Use (21 CFR 801 Subpart C)
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3
K241248 Page 1 of 4
Image /page/3/Picture/1 description: The image shows the logo for Spectrum Medical. The word "Spectrum" is written in blue, followed by a red line that resembles a heartbeat. The word "Medical" is written in blue after the red line.
Spectrum Medical S.r.l. Via di Mezzo, 23 41037 Mirandola (MO) Tel: +39 0535 1803050 FAX: +39 0535 1803051
510(K) SUMMARY
l. SUBMITTER
| Submitter Name: | Spectrum Medical S.r.l. |
|---|---|
| Submitter Address: | Via di Mezzo, 23 41037 Mirandola (MO) Italy |
| Contact Person: | Raffaella Tommasini, QA&RA Director |
| Spectrum Medical S.r.l. | |
| Phone: | +39 0535 1803050 |
| e-mail: | raffaella.tommasini@spectrummedical.com |
| Fax: | +39 0535 1803051 |
| Date Summary Prepared: | May 03, 2024 |
II. DEVICE
Proprietary Name: Common Name: Classification Name:
Regulatory Class: Product Code: Panel:
Quantum Perfusion Dual Lumen Cannula 31F-V1 Dual Lumen Cannula 31F-V1 Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass ll DFW Cardiovascular Devices, Office of office office Health Technology 2 (OHT2) / Division of Health Technology 2 B (Circulatory Support, Structural and Vascular Devices)
4
Image /page/4/Picture/0 description: The image shows the logo for Spectrum Medical. The word "Spectrum" is written in blue, followed by a red line that resembles a heart rate monitor. The word "Medical" is written in blue after the red line.
Spectrum Medical S.r.l. Via di Mezzo, 23 41037 Mirandola (MO) Tel: +39 0535 1803050 FAX: +39 0535 1803051
III. PREDICATE DEVICES
| Proprietary Name: | Quantum Perfusion Dual Lumen Cannula 31F |
|---|---|
| Common Name: | Dual Lumen Cannula 31F |
| Registered Establishment Name: | Spectrum Medical S.r.l |
| Classification Name: | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Regulatory Class: | II |
| Product Code: | DWF |
| Panel: | Cardiovascular Devices, Office of Health Technology 2 (OHT2) / Division of Health Technology 2 B (Circulatory Support, Structural and Vascular Devices) |
| 510(k) Number: | K221353 |
IV. DEVICE DESCRIPTION
Quantum Perfusion Dual Lumen Cannula product family are single use devices intended to be used in medical procedures providing cardiac and/or respiratory support up to 6 hours. Devices are characterized by two coaxial catheters and are designed to be coupled with an extracorporeal circuit for artificial oxygenation of the blood and carbon dioxide removal.
Devices exploit a single site insertion which reduces the invasiveness of extracorporeal procedures. It can be inserted via a percutaneous approach through the right internal jugular vein. Blood is drained through the lumen of the outer catheter and returned through the lumen of the inner catheter.
Devices feature multiple inflow openings in the outer catheter limiting the circulation of unoxygenated blood.
Devices are non-toxic, non-pyrogenic, sterilized by ethylene oxide and packaged in a double pouch. All the devices' surfaces in contact with blood are coated with a phosphorylcholine-based biocompatible material.
V. INTENDED USE / INDICATIONS FOR USE
The Quantum Perfusion Dual Lumen Cannula is intended for use as a single cannula for both venous drainage and reinfusion of blood via the internal jugular vein during extracorporeal life support procedures for periods of maximum 6 hours.
5
Image /page/5/Picture/0 description: The image shows the logo for Spectrum Medical. The text "Spectrum" is in blue, followed by a red line that resembles a heartbeat. The text "Medical" is in blue and follows the red line. The logo is simple and professional.
Spectrum Medical S.r.I. Via di Mezzo. 23 41037 Mirandola (MO) Tel: +39 0535 1803050 FAX: +39 0535 1803051
VI. COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICE
One additional device model has been introduced in the Dual Lumen Cannula product family in order to provide to clinicians/users an additional option to perform cardiopulmonary bypass procedures.
New REF code introduced in the portfolio Quantum Perfusion Dual Lumen Cannula product family is aligned with information provided in original submission K221353 in terms of general structure, principles of operation, intended use, manufacturing and sterilization process.
Technical specifications have been verified through testing activities performed according to the same internal applicable standards/protocols of the original cleared devices.
Applicable testing activities demonstrated that the proposed device model does not raise any issues of safety and effectiveness as compared to the currently cleared predicate device.
VII. PERFORMANCE DATA
NON-CLINICAL TESTING
The following activities were performed to demonstrate product safety and effectiveness, considering the proposed change and related impact:
- -Update of labeling and Instructions for Use (IFU) according to ISO 15223-1:2021 Medical Devices - Symbols to Be Used with Medical Device Labels, Labelling, And Information to Be Supplied - Part 1: General Requirements [Recognition Nr. 5-134];
- -Performance tests for new REF codes introduced in the portfolio, according to applicable Recognized Consensus Standard ISO 18193:2021 [Recognition Nr. 3-176].
Animal Study
No animal studies have been performed to support changes object of the present Special 510(k).
6
Image /page/6/Picture/0 description: The image shows the logo for Spectrum Medical. The text "Spectrum Medical" is written in blue, with the word "Spectrum" appearing to the left of a red heartbeat symbol. The word "Medical" is written to the right of the heartbeat symbol.
Spectrum Medical S.r.l. Via di Mezzo, 23 41037 Mirandola (MO) Tel: +39 0535 1803050 FAX: +39 0535 1803051
CLINICAL TESTING
No clinical data have been included in the current 510(k) submission to support substantial equivalence to legally marketed predicate devices.
VIII. CONCLUSIONS
Considering all changes performed on original devices cleared K221353 as described in Section "Device Description" of current submission, it could be stated that devices under evaluation are identical in terms of intended use and applicable medical technique.
Based on the testing activities, technological characteristics and the indications for use, the proposed devices have been demonstrated to be appropriate for their intended use and are considered substantially equivalent to Spectrum Medical s.r.l. own original devices.