Search Results
Found 1 results
510(k) Data Aggregation
(181 days)
PCI Guide Wires are intended to facilitate the placement of balloon dilatation catheters during percutaneous coronary intervention (PCI) and percutaneous transluminal angioplasty (PTA).
The PCI Guide Wires are not intended for use in the neurovasculature.
The MINAMO consists of a hybrid NiTi and stainless-steel core wire and a coil assembly on the distal end of the device. The coil assembly is soldered to the NiTi portion of the core. In addition, coatings are applied on the surface of the MINAMO. The proximal portion is coated with PTFE. The distal section is coated with hydrophilic coating, with the distal tip coated with silicone. The MINAMO is available in both 190cm and 300cm lengths and with different tip shapes.
The MINAMO is a coronary guide wire. The 510(k) summary provides details about non-clinical testing performed to demonstrate substantial equivalence to predicate devices.
1. Table of Acceptance Criteria and Reported Device Performance:
The document broadly states that "The in vitro bench tests demonstrated that the MINAMO met all acceptance criteria and performed similarly to the predicate devices." Specific numerical acceptance criteria values and reported device performance values are generally not detailed in 510(k) summaries for non-clinical tests. This is a common practice, as the focus is on demonstrating that the device meets established performance thresholds and is comparable to previously cleared devices.
Test / Assessment | Acceptance Criteria (General Description) | Reported Device Performance (General Description) |
---|---|---|
Dimensional verification / Appearance | Met specified dimensions and visual criteria. | Met all acceptance criteria. |
Tensile Strength | Met specified strength requirements, comparable to predicate. | Met all acceptance criteria. |
Torque Strength | Met specified torque performance requirements, comparable to predicate. | Met all acceptance criteria. |
Torqueability | Demonstrated appropriate torque transmission, comparable to predicate. | Met all acceptance criteria. |
Tip Flexibility | Met specified flexibility characteristics, comparable to predicate. | Met all acceptance criteria. |
Coating Adhesion | Met specified adhesion strength requirements, comparable to predicate. | Met all acceptance criteria. |
Catheter Compatibility | Demonstrated compatibility with standard catheters. | Met all acceptance criteria. |
Lubricity | Met specified lubricity requirements, comparable to predicate. | Met all acceptance criteria. |
Corrosion Resistance | Demonstrated resistance to corrosion under specified conditions. | Met all acceptance criteria. |
Kink Resistance | Met specified kink resistance requirements, comparable to predicate. | Met all acceptance criteria. |
Radiodetectability | Demonstrated adequate visibility under fluoroscopy. | Met all acceptance criteria. |
Coating Integrity / Acute Particulate Characterization | Maintained coating integrity and minimal particulate release. | Met all acceptance criteria. |
Packaging / Transportation assessment | Maintained device integrity through packaging and simulated transport. | Met all acceptance criteria. |
Biocompatibility Tests (Cytotoxicity, Sensitization, Intracutaneous Irritation, Systemic Toxicity, USP Rabbit Pyrogen, Material Mediated, Hemolysis, Partial Thromboplastin Time, In Vivo Thromboresistance, Sc5b-9 Complement Activation) | Met international standards for biocompatibility (e.g., ISO 10993). | Met all acceptance criteria. |
2. Sample Size Used for the Test Set and Data Provenance:
The document does not specify the exact sample sizes used for each individual non-clinical test. It generally refers to "non-clinical laboratory testing." For medical devices, these tests are typically performed in a laboratory setting, and the provenance is the company's internal R&D or a contract testing lab. These are all retrospective tests conducted on manufactured device samples. There is no information regarding country of origin for the data for non-clinical bench testing, but the applicant's headquarters are in Japan.
3. Number of Experts Used to Establish Ground Truth and Qualifications:
This information is not applicable to the non-clinical bench testing described. These tests do not involve human interpretation or the establishment of ground truth by clinical experts in the same way an AI diagnostic device would. Performance is measured against physical and chemical specifications.
4. Adjudication Method:
This information is not applicable. Adjudication methods are typically used in clinical studies or studies involving human readers, which is not the nature of the reported performance data.
5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study:
An MRMC study was not done. The device is a physical medical instrument (guide wire), not an AI diagnostic tool.
6. Standalone Performance Study:
A standalone performance study was not done in the context of an AI algorithm. The reported tests are for the physical properties and performance of the guide wire itself. The document describes "non-clinical laboratory testing" which inherently is a standalone evaluation of the device against predefined specifications.
7. Type of Ground Truth Used:
The "ground truth" for the non-clinical tests is established by:
- Engineering Specifications: Predetermined physical and chemical properties that an equivalent guide wire must possess (e.g., specific tensile strength, flexibility parameters, corrosion resistance).
- International Standards: Adherence to relevant ISO standards (e.g., for biocompatibility, sterility) or equivalent national standards.
- Predicate Device Performance: Demonstrating comparable performance to legally marketed predicate devices through comparative bench testing.
8. Sample Size for the Training Set:
This information is not applicable. The MINAMO is a physical medical device, not an AI or machine learning algorithm that requires a training set.
9. How the Ground Truth for the Training Set Was Established:
This information is not applicable, as there is no training set for a physical guide wire.
Ask a specific question about this device
Page 1 of 1