(187 days)
No
The device description focuses on the physical components and materials of a steerable guide wire. There is no mention of software, algorithms, image processing, AI, ML, or any data-driven functionalities. The performance studies described are bench tests, not studies involving AI/ML model training or evaluation.
No
The device is a guidewire designed to direct a catheter, which is a diagnostic or interventional procedure rather than a therapeutic one itself. Its function is to facilitate the delivery of other instruments, not to treat a condition.
No
This device is a guide wire, which is an interventional tool used to navigate catheters within the vasculature. While it can be used during "diagnostic or interventional procedures," its function is not to diagnose conditions itself but rather to facilitate other diagnostic or interventional instruments.
No
The device description clearly outlines a physical guide wire made of various materials with coatings, indicating it is a hardware device, not software-only.
No, 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, tissue) to provide information about a person's health. These tests are performed outside the body.
- Device Description and Intended Use: The description clearly states that this device is a steerable guide wire intended to direct a catheter within the anatomical vasculature. This is an invasive medical device used inside the body during a procedure.
- Lack of Diagnostic Testing: There is no mention of this device being used to analyze samples or perform any kind of diagnostic test on bodily fluids or tissues. Its function is purely mechanical – guiding a catheter.
Therefore, based on the provided information, the CROSSLEAD 0.018inch is a medical device, but it falls under the category of an invasive surgical/interventional device, not an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
This product is intended to direct a catheter to the desired anatomical vasculature (excluding coronary and cerebral vessels) during diagnostic or interventional procedures.
Product codes
DQX
Device Description
The CROSSLEAD 0.018inch is steerable guide wire with a maximum diameter of 0.46mm (0.018inches) and available in various lengths of 100 cm, 200 cm, 235 cm and 300 cm. The quide wire consists of a hybrid nitinol (Ni-Ti) and stainlesssteel (SUS) core wire with a stainless steel inner coil, a stainless steel and Platinum-Nickel (Pt-Ni) outer coil. The coil is radiopaque to achieve visibility and can be made to bend easily to accommodate vessel tortuosity. A hydrophilic and polyurethane coating are applied to the distal portion of the guide wire. A hydrophobic coating (PTFE) is applied to proximal portion. The purpose of these surface coatings is to provide lubricity when the guide wire is passed through percutaneous catheters.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
peripheral vasculature (excluding coronary and 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)
Non-clinical laboratory testing was performed on the CROSSLEAD 0.018inch to determine substantial equivalence. The following testing/assessments were conducted:
- Tensile Strength
- Torque Strength
- Torqueability
- Tip Flexibility
- Coating Integrity
- Catheter Compatibility
- Visual Inspection
- Corrosion Resistance
- Kink Resistance
- Radio - Detectability
- Dimensional Verification
- Coating Integrity / Particulate Characterization
The in vitro bench tests demonstrated that the CROSSLEAD 0.018inch met all acceptance criteria and performed similarly to the predicate and reference devices. Performance data demonstrates the CROSSLEAD 0.018inch functions as intended and has a safety and effectiveness profile that is similar to the predicate and reference devices although there are the technological differences between the subject and predicate/reference devices.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 870.1330 Catheter guide wire.
(a)
Identification. A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.(b)
Classification. Class II (special controls). The device, when it is a torque device that is manually operated, non-patient contacting, and intended to manipulate non-cerebral vascular guide wires, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 870.9.
0
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA acronym along with the full name of the agency on the right. The Department of Health & Human Services logo features a stylized human figure, while the FDA part includes the acronym "FDA" in a blue square, followed by "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
March 5, 2025
Asahi Intecc Co., Ltd. Cynthia Valenzuela Director, Quality Systems, Regulatory Affairs/Compliance Asahi Intecc USA, Inc. 3002 Dow Avenue Suite 212 Tustin, California 92780
Re: K242597
Trade/Device Name: CROSSLEAD 0.018inch Regulation Number: 21 CFR 870.1330 Regulation Name: Catheter Guide Wire Regulatory Class: Class II Product Code: DQX Dated: August 30, 2024 Received: August 30, 2024
Dear Cynthia Valenzuela:
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.
1
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).
Your device is also subject to, among other requirements, the Quality System (OS) 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 QS 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.
All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-device-advicecomprehensive-regulatory-assistance/unique-device-identification-system-udi-system.
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-regulatory
2
assistance/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,
Jenny R.
Katsnelson -S
Digitally signed by Jenny R.
Katsnelson -S
Date: 2025.03.05 23:14:13
-05'00'
for Lydia Glaw Assistant Director DHT2C: Division of Coronary and Peripheral Intervention Devices OHT2: Office of Cardiovascular Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
3
Indications for Use
510(k) Number (if known) K242597
Device Name CROSSLEAD 0.018inch
Indications for Use (Describe)
This product is intended to direct a catheter to the desired anatomical vasculature (excluding coronary and cerebral vessels) during diagnostic or interventional procedures.
| Type of Use (Select one or both, as applicable) | |
|---|---|
| ------------------------------------------------- | -- |
X Prescription Use (Part 21 CFR 801 Subpart D)
| Over-The-Counter Use (21 CFR 801 Subpart C)
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4
K242597 Page 1 of 6
510(k) Summary (as required by 21 CFR § 807.92) ΛՏΛΗΙ INTECC CO.,LTD. Global Headquarters and R&D Center
3-100 Akatsuki-cho, Seto-shi, Aichi 489-0071 Japan TEL:+81-561-48-5551 FAX:+81-561-48-5552 http://www.asahi-intecc.co.jp/
CROSSLEAD 0.018inch
510(k) 242597
| Date Prepared: | 30 AUG 2024 | |
|---|---|---|
| Applicant: | ASAHI INTECC CO., LTD. | |
| 3-100 Akatsuki-cho, | ||
| Seto, Aichi 489-0071 Japan | ||
| Contact: | Mrs. Cynthia Valenzuela | |
| Director, Quality and Regulatory Affairs | ||
| ASAHI INTECC USA, Inc. | ||
| 3002 Dow Avenue, Suite 212 | ||
| Tustin, CA 92780 | ||
| Tel: (949) 745-1617 | ||
| e-mail: cynthiav@asahi-intecc-us.com | ||
| Trade Name: | CROSSLEAD 0.018 inch | |
| Device Classification: | Class 2 per 21 CFR § 870.1330 | |
| Classification Name: | Catheter, Guide, Wire | |
| Product Code: | DQX - Catheter Guide Wire | |
| Predicate Device: | Gladius Mongo18 PV ES | K213868 |
| Reference Devices: | CROSSLEAD Tracker | K241510 |
| CROSSLEAD Penetration | K230377 | |
| V-18 Control Wire | K033742 |
5
INTENDED USE/INDICATIONS FOR USE:
This product is designed to direct a catheter to the desired anatomical location in the peripheral vasculature (excluding coronary and cerebral vessels) during diagnostic or interventional procedures.
DEVICE DESCRIPTION:
The CROSSLEAD 0.018inch is steerable guide wire with a maximum diameter of 0.46mm (0.018inches) and available in various lengths of 100 cm, 200 cm, 235 cm and 300 cm. The quide wire consists of a hybrid nitinol (Ni-Ti) and stainlesssteel (SUS) core wire with a stainless steel inner coil, a stainless steel and Platinum-Nickel (Pt-Ni) outer coil. The coil is radiopaque to achieve visibility and can be made to bend easily to accommodate vessel tortuosity. A hydrophilic and polyurethane coating are applied to the distal portion of the guide wire. A hydrophobic coating (PTFE) is applied to proximal portion. The purpose of these surface coatings is to provide lubricity when the guide wire is passed through percutaneous catheters.
The basic structure, construction and materials of the CROSSLEAD 0.018inch are similar to those of the predicate Gladius Mongo18 PV ES (K213868), and the references CROSSLEAD Penetration (K230377), CROSSLEAD Tracker (K241510) and V-18 Control Wire (K033742).
COMPARISON WITH PREDICATE AND REFERENCE DEVICES:
The following comparison table of the CROSSLEAD 0.018inch and the predicate/reference devices indicates that the technological characteristics of the subject device such as the components, design, materials, sterilization method and operating principle are similar. The intended use of the CROSSLEAD 0.018inch and its predicate device is also comparable.
The following technological differences exist between the subject and predicate/reference devices:
- Outer Coil structure ●
- Core shaft structure
6
| Subject | Predicate | References | |||
|---|---|---|---|---|---|
| Device name | CROSSLEAD 0.018inch | Gladius Mongo18 PV ES | CROSSLEAD Tracker | CROSSLEAD Penetration | V-18 Control Wire |
| 510(k) | TBD | K213868 | K241510 | K230377 | K033742 |
| Manufacturer | ASAHI INTECC CO., LTD. | Boston Scientific | |||
| Intended and/or | |||||
| Indication for Use | This product is intended | ||||
| to direct a catheter to | |||||
| the desired anatomical | |||||
| location in the | |||||
| peripheral vasculature | |||||
| (excluding coronary and | |||||
| cerebral vessels) during | |||||
| diagnostic or | |||||
| interventional | |||||
| procedures. | This product is intended | ||||
| to facilitate the | |||||
| placement and exchange | |||||
| of diagnostic and | |||||
| therapeutic devices | |||||
| during intravascular | |||||
| procedures. This device is | |||||
| intended for peripheral | |||||
| vascular use only. | This product is designed | ||||
| to direct a catheter to | |||||
| the desired anatomical | |||||
| location in the | |||||
| peripheral vasculature | |||||
| during diagnostic or | |||||
| interventional procedures. | |||||
| Do not use the guide wire | |||||
| in neurovascular. | This product is designed | ||||
| to direct a catheter | |||||
| to the desired anatomical | |||||
| location in the peripheral | |||||
| vasculature during | |||||
| diagnostic or | |||||
| interventional procedures. | The 110cm V-18 | ||||
| Control Wire is | |||||
| intended for general | |||||
| intravascular use | |||||
| including the | |||||
| placement of PTA | |||||
| balloon catheters | |||||
| requiring an 0.018" | |||||
| guide wire in | |||||
| hemodialysis AV access | |||||
| procedures. The wire | |||||
| can be torqued to | |||||
| facilitate placement of | |||||
| diagnostic or | |||||
| therapeutic catheters. | |||||
| This device is intended | |||||
| for peripheral vascular | |||||
| use only. A torque | |||||
| device is included with | |||||
| each wire to facilitate | |||||
| directional | |||||
| manipulation of the | |||||
| guide wire. |
7
| Subject | Predicate | References | |||
|---|---|---|---|---|---|
| Device name | CROSSLEAD 0.018inch | Gladius Mongo18 PV | |||
| ES | CROSSLEAD Tracker | CROSSLEAD | |||
| Penetration | V-18 Control Wire | ||||
| Nominal OD | 0.46mm | ||||
| (0.018") | 0.46mm | ||||
| (0.018") | 0.36mm | ||||
| (0.014") | 0.36mm(0.014") | ||||
| 0.46mm(0.018") | 0.46mm | ||||
| (0.018") | |||||
| Usable Length | 100cm, 200cm, | ||||
| 235cm, 300cm | 190cm, 235cm, 300cm | 100cm, 200cm, | |||
| 235cm, 300cm | 200cm, 235cm, | ||||
| 300cm | 110cm, 150cm, | ||||
| 200cm, 300cm | |||||
| Outer Coil | Austenitic Stainless | ||||
| Steel | |||||
| Pt-Ni alloy | Pt-Ni alloy | Austenitic Stainless | |||
| Steel | |||||
| Pt-Ni alloy | Pt-Ni alloy | unknown | |||
| Inner Coil | Austenitic Stainless | ||||
| Steel | Austenitic Stainless | ||||
| Steel | Pt-Ni alloy | - | unknown | ||
| Taper Core Wire | Ni-Ti alloy | ||||
| Austenitic Stainless | |||||
| Steel | Austenitic Stainless | ||||
| Steel | Ni-Ti alloy | ||||
| Austenitic Stainless | |||||
| Steel | Austenitic Stainless | ||||
| Steel | Stainless Steel | ||||
| Tip Shape | Straight, Pre-shape | Straight, Pre-shape | Straight, Pre-shape | Straight, Pre-shape | Straight |
| Coating | Hydrophilic | ||||
| Polyurethane | |||||
| PTFE | Hydrophilic | ||||
| Polyurethane | |||||
| PTFE | Hydrophilic | ||||
| Polyurethane | |||||
| PTFE | Hydrophilic | ||||
| PTFE | Hydrophilic | ||||
| PTFE | |||||
| Polyurethane | |||||
| Polymer | |||||
| Solder | Ag-Sn | ||||
| Au-Sn | Ag-Sn | ||||
| Au-Sn | Ag-Sn | ||||
| Au-Sn | Au-Sn | unknown | |||
| Sterilization | Ethylene oxide | ||||
| SAL 10-6 | Ethylene oxide | ||||
| SAL 10-6 | Ethylene oxide | ||||
| SAL 10-6 | Ethylene oxide | ||||
| SAL 10-6 | unknown |
8
NON-CLINICAL TESTING/PERFORMANCE DATA:
Non-clinical laboratory testing was performed on the CROSSLEAD 0.018inch to determine substantial equivalence. The following testing/assessments were conducted:
- Tensile Strength ●
- . Torque Strength
- Torqueability .
- Tip Flexibility ●
- Coating Integrity
- Catheter Compatibility ●
- Visual Inspection
- Corrosion Resistance
- Kink Resistance ●
- Radio - Detectability
- Dimensional Verification ●
- Coating Integrity / Particulate Characterization ●
The in vitro bench tests demonstrated that the CROSSLEAD 0.018inch met all acceptance criteria and performed similarly to the predicate and reference devices. Performance data demonstrates the CROSSLEAD 0.018inch functions as intended and has a safety and effectiveness profile that is similar to the predicate and reference devices although there are the technological differences between the subject and predicate/reference devices.
BIOCOMPATIBILITY:
The biocompatibility of the CROSSLEAD 0.018inch had been confirmed in regards to the following aspects.
- Cytotoxicity
- Sensitization
- Intracutaneous Irritation ●
- Systemic Toxicity ●
- Material Mediated Pyrogenicity ●
- Hemolvsis ●
- Partial Thromboplastin Time .
- Sc5b-9 Complement Activation
- In Vivo Thromboresistance .
9
CONCLUSION:
The CROSSLEAD 0.018inch and the predicate/reference devices share the same intended use and the same or similar technological characteristics such as components, design, materials, sterilization method and operating principles. Differences in technological characteristics between the subject and predicate/reference devices do not raise different questions of safety and effectiveness. Non- clinical tests demonstrate that the device has a similar safety and effectiveness profile as the legally marketed predicate/reference devices. Therefore, ASAHI considers the CROSSLEAD 0.018inch to be substantially equivalent to the predicate and reference devices.