(25 days)
No reference devices were used in this submission.
No
The device description and performance studies focus on the physical characteristics and functionality of a microcatheter for delivering materials. There is no mention of AI, ML, image processing, or any software-driven analytical capabilities.
No
This device is a microcatheter used to deliver diagnostic, embolic, or therapeutic materials, but it is not a therapeutic device itself. Its function is to facilitate the delivery of other substances that may have therapeutic effects.
No
The device is a microcatheter used for accessing subselective regions and infusing materials. While it can be used for the infusion of "diagnostic materials," the device itself does not perform a diagnostic function; it is a delivery tool.
No
The device description clearly details a physical microcatheter with specific dimensions, materials (hydrophilic coating, radiopaque marker), and physical components (hub, strain relief). The performance studies also focus on bench testing of physical characteristics and functionality, not software performance.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for the controlled and selective infusion of diagnostic, embolic, or therapeutic materials into vessels. This is an in vivo application, meaning it's used within the living body.
- Device Description: The description details a physical catheter designed for insertion into the vasculature.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens derived from the human body (like blood, urine, tissue, etc.) outside of the body to provide information for diagnostic purposes.
IVD devices are used to perform tests on samples taken from the body to diagnose diseases or conditions. This microcatheter is a tool for delivering substances directly into the body for treatment or imaging, which is a different category of medical device.
N/A
Intended Use / Indications for Use
The Microcatheter is intended for general intravascular use, including peripheral and coronary vasculature. Once the subselective region has been accessed, the microcatheter can be used for the controlled and selective infusion of diagnostic, embolic or therapeutic materials into vessels. The catheter should not be used in the cerebral vessels.
Product codes (comma separated list FDA assigned to the subject device)
KRA
Device Description
The Maestro Microcatheter is available in 2.8F (proximal) / 2.1F (distal) size and 110cm, 130cm and 150cm lengths. The distal tip of the microcatheter is offered in straight or pre-shaped 45 degree and swan neck configurations. The proximal end of the catheter consists of a molded winged hub with a tapered strain relief. The outer surface of the distal 80cm of the microcatheter shaft is coated with a hydrophilic coating designed to facilitate the introduction of the catheter into the vasculature. The microcatheter incorporates a radiopaque marker at the distal tip to facilitate fluoroscopic visualization. The Maestro Microcatheter is offered with two 3ml syringes.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Fluoroscopic visualization
Anatomical Site
Peripheral and coronary vasculature. The catheter should not be used in the cerebral vessels.
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)
Performance Testing-Bench
- Surface
- Tensile Force
- Dimensions
- Radio-detectability
- Freedom from Liquid Leakage
- Flow Rate
- Kink Resistance
- Lubricity
- Coating Coverage
- Delivery of Microspheres and Particles
- Torque Strength
- Particulate
- Tip Shape Retention
- Hub Migration from Clip
Design Validation
- Delivery of Coils
- Guidewire Compatibility
- Catheter Compatibility
- Torsion
- Negative Pressure Collapse
- Hoop Removal
- Distal Tip
- Tip Straightener
- Soft Distal Section
- Trackability
- Pushability
- Reposition of Guidewire
The results of the testing demonstrated that the subject 2.8F/2.1F Maestro Microcatheter met the predetermined acceptance criteria applicable to the safety and efficacy of the device. This has demonstrated the subject is substantially equivalent to the predicate device.
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.
No reference devices were used in this submission.
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
§ 870.1210 Continuous flush catheter.
(a)
Identification. A continuous flush catheter is an attachment to a catheter-transducer system that permits continuous intravascular flushing at a slow infusion rate for the purpose of eliminating clotting, back-leakage, and waveform damping.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/2 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" around the perimeter. Inside the circle is an abstract symbol of three human profiles facing to the right, stacked on top of each other.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - W 066-G609 Silver Spring, MD 20993-0002
August 4, 2017
Merit Medical Systems, Inc. Niloufar Samimi Regulatory Affairs Specialist II 1600 West Merit Parkway South Jordan, Utah 84095
Re: K172081
Trade/Device Name: Maestro Microcatheter Regulation Number: 21 CFR 870.1210 Regulation Name: Continuous Flush Catheter Regulatory Class: Class II Product Code: KRA Dated: July 6, 2017 Received: July 10, 2017
Dear Niloufar Samimi:
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. 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.
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 device
1
related 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.
M. G. Hillemann
for Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Indications for Use
Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement below.
..
510(k) Number (if known)
Device Name Maestro Microcatheter
Indications for Use (Describe)
The Microcatheter is intended for general intravascular use, including peripheral and coronary vasculature. Once the subselective region has been accessed, the microcatheter can be used for the controlled and selective infusion of diagnostic, embolic or therapeutic materials into vessels. The catheter should not be used in the cerebral vessels.
| 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) |
|---|---|
| ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- | ------------------------------------------------------------------------------------------------------------- |
CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the
time to review instructions, search existing data sources, gather and maintain the data needed and complete
and review the collection of information. Send comments regarding this burden estimate or any other aspect
of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services
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information unless it displays a currently valid OMB number."
FORM FDA 3881 (8/14)
Page 1 of 1
PSC Publishing Services (101) 443-6740 EF
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510(k) Summary
| General
Provisions | Submitter Name:
Address:
Telephone Number:
Contact Person:
Date Prepared:
Registration Number: | Merit Medical Systems, Inc.
1600 West Merit Parkway
South Jordan, UT 84095
(801) 208-4583
Niloufar Samimi
07/05/2017
1721504 |
|------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Subject Device | Trade Name:
Common/Usual Name:
Classification Name:
Regulatory Class:
Product Code:
21 CFR §:
Review Panel: | Maestro Microcatheter
Microcatheter
Continuous Flush Catheter
2
KRA
870.1210
Cardiovascular |
| Predicate Device | Trade Name:
Classification Name:
Premarket Notification:
Manufacturer: | Maestro Microcatheter
Continuous Flush Catheter
K082613
Merit Medical Systems, Inc.
This predicate has not been subject to a design-related recall |
| Reference Device | No reference devices were used in this submission. | |
| Device
Description | The Maestro Microcatheter is available in 2.8F (proximal) / 2.1F (distal)
size and 110cm, 130cm and 150cm lengths. The distal tip of the
microcatheter is offered in straight or pre-shaped 45 degree and swan
neck configurations. The proximal end of the catheter consists of a
molded winged hub with a tapered strain relief. The outer surface of
the distal 80cm of the microcatheter shaft is coated with a hydrophilic
coating designed to facilitate the introduction of the catheter into the
vasculature. The microcatheter incorporates a radiopaque marker at
the distal tip to facilitate fluoroscopic visualization.
The Maestro Microcatheter is offered with two 3ml syringes. | |
| Indications for
Use | There is no change in the Indications for Use Statement from the
predicate to the subject device.
The Microcatheter is intended for general intravascular use, including
peripheral and coronary vasculature. Once the subselective region has
been accessed, the microcatheter can be used for the controlled and
selective infusion of diagnostic, embolic or therapeutic materials into
vessels. The catheter should not be used in the cerebral vessels. | |
4
The design and technological characteristics of the subject 2.8F/2.1F Maestro Microcatheter are substantially equivalent to those of the predicate Maestro Microcatheter. The subject device has the same basic design as the predicate device. The main difference between the subject and the predicate devices is in the French size to expand the product line to include the 2.8F/2.1F microcatheter. The comparison between the subject and the predicate devices is based on the following:
- Same intended use ●
- . Same indications for use
- Similar material types that meet ISO 10993 biocompatibility . requirements
- Same design
- Same sterilization methods ●
- Same fundamental technology/principle of operation ●
No performance standards have been established under Section 514 of the Food. Drug and Cosmetic Act for these devices. Performance testing of the subject 2.8F/2.1F Maestro Microcatheter was conducted based on the risk analysis and based on the requirements of the following international standard:
- ISO 10555-1:2013, Intravascular Catheters Sterile and single-● use catheters - Part 1: General requirements
- ISO 11135:2014, Sterilization of health care products Ethylene ● oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
- ISO 10993-1:2009. Biological Evaluation of Medical Devices . Part 1: Evaluation and Testing within a risk management process, and FDA guidance Required Biocompatibility Training and Toxicology Profiles for Evaluation of Medical Devices, May 1, 1995
- ISO 10993-7:2008, Biological evaluation of medical devices -● Part 7: Ethylene oxide sterilization residuals
- ISO 2233:2000, Packaging complete, filled transport ● packages and unit loads - conditioning for testing
- ASTM D4169-14:2014, Standard practice for performance ● testing of shipping containers and systems
Comparison to Predicate Device
5
The following tests were performed to demonstrate there were no unacceptable risks associated with the changes made to the device:
Performance Testing-Bench
- Surface ●
- Tensile Force ●
- Dimensions ●
- . Radio-detectability
- Freedom from Liquid Leakage ●
- Flow Rate
- Kink Resistance ●
- Lubricity ●
- Coating Coverage ●
- Delivery of Microspheres and Particles ●
- Torque Strength ●
- Particulate ●
- Tip Shape Retention
- Hub Migration from Clip ●
Safety & Performance Tests cont.
Design Validation
- Delivery of Coils ●
- Guidewire Compatibility ●
- Catheter Compatibility ●
- Torsion ●
- Negative Pressure Collapse .
- Hoop Removal ●
- Distal Tip
- Tip Straightener ●
- Soft Distal Section
- Trackability ●
- Pushability ●
- Reposition of Guidewire .
The results of the testing demonstrated that the subject 2.8F/2.1F Maestro Microcatheter met the predetermined acceptance criteria applicable to the safety and efficacy of the device. This has demonstrated the subject is substantially equivalent to the predicate device.
6
| Summary of
Substantial
Equivalence | Based on the indications for use, design, safety and performance
testing, the subject 2.8F/2.1F Maestro Microcatheter meets the
requirements that are considered essential for its intended use and is
substantially equivalent to the predicate device, the Maestro
Microcatheter, K082613, manufactured by Merit Medical Systems, Inc |
| ------------------------------------------ | ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- |
|---|