(63 days)
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No
The document describes a physical medical device (guide wire) and its mechanical properties, with no mention of software, algorithms, or data processing that would indicate AI/ML.
No
The device is described as facilitating the placement and exchange of therapeutic devices, but is not itself a therapeutic device.
No
This device is a guide wire intended to facilitate the placement and exchange of other therapeutic devices during interventional procedures, which is a functional role for conducting a procedure, not for diagnosing a condition.
No
The device description clearly describes a physical guide wire with various material components and configurations, indicating it is a hardware device, not software only.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the guide wires are used to "facilitate the placement and exchange of balloon dilatation catheters or other therapeutic devices during PTCA or other intravascular interventional procedures." This describes a device used in vivo (within the body) to assist in a medical procedure.
- Device Description: The description details the physical characteristics of a guide wire designed to be inserted into blood vessels.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (like blood, urine, or tissue) in vitro (outside the body) to provide information for diagnosis, monitoring, or screening.
IVD devices are used to perform tests on samples taken from the body, while this device is used directly within the body during a procedure.
N/A
Intended Use / Indications for Use
The SCIMED ChoICE™ Guide Wires are intended to facilitate the placement and exchange of balloon dilatation catherers or other therapeutic devices during PTCA or other intravascular interventional procedures. The ChoICE™ Guide Wire family is not intended for use in the cerebral vasculature. The devices are provided sterile and intended for one procedure only.
Product codes
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Device Description
The ChoICE, ChoICE Plus, and ChoICE Exchange PTCA Guide Wires are steerable guide wires available in a nominal diameter of 0.014 inches and two tip configurations, straight shapeable and pre-formed J-Tip. The four tip flexibilities available will be Floppy, Intermediate, Standard, and Extra Support. A polymer sleeve, extending from the spring coil to the proximal fluorinated polymer coated core wire, surrounds the tapered core wire and is coated with ICE™ Hydrophilic Coating. The available lengths for the guide wires will be ChoICE-190 cm, ChoICE Plus-182 cm and ChoICE Exchange-300 centimeters.
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
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Indicated Patient Age Range
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Intended User / Care Setting
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Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies
Non-Clinical Test Summary: Testing and evaluation of the guide wires included ICE lubricious coating adherence, polyurethane shear strength, polyurethane adherence, and proximal spring coil joint shear testing. In addition, shelf life testing was performed on test units with the modified polyurethane material. Test results verified that the modified ChoICE, ChoICE Plus, and ChoICE Exchange met the design requirements and are adequate for their intended use. Torque testing also performed.
Key Metrics
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Predicate Device(s)
SCIMED ChoICE™ PTCA Guide Wire, SCIMED ChoICE™ Plus PTCA Guide Wire, SCIMED ChoICE™ Exchange PTCA Guide Wire
Reference Device(s)
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Predetermined Change Control Plan (PCCP) - All Relevant Information
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§ 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
510(K) Notification SCIMED ChoICE, ChoICE Plus, ChoICE Exchange PTCA Guide Wires Page 3
SECTION THREE--SUMMARY OF SAFETY AND EFFECTIVENESS
510(K) SUMMARY OF SAFETY AND EFFECTIVENESS (Pursuant To Section 12 of the SAFE MEDICAL DEVICES ACT of 1990) Prepared March 12, 1996
| General Provisions:
Submitter's Name and Address: | SCIMED Life Systems, Inc.
One SCIMED Place
Maple Grove, Minnesota 55311 |
|------------------------------------------------------|------------------------------------------------------------------------------------------------------------------|
| Contact Person: | Connie J. Del Toro
(612) 494-2656 |
| Classification Name: | Catheter Guide Wire |
| Common or Usual Name: | PTCA Guide Wire |
| Proprietary Name: | SCIMED ChoICE™ PTCA Guide Wire
SCIMED ChoICE™ Plus PTCA Guide Wire
SCIMED ChoICE™ Exchange PTCA Guide Wire |
Name of Predicate Devices: II.
SCIMED ChoICE™ PTCA Guide Wire SCIMED ChoICE™ Plus PTCA Guide Wire SCIMED ChoICE™ Exchange PTCA Guide Wire
III. Device Description:
I
The ChoICE, ChoICE Plus, and ChoICE Exchange PTCA Guide Wires are steerable guide wires available in a nominal diameter of 0.014 inches and two tip configurations, straight shapeable and pre-formed J-Tip. The four tip flexibilities available will be Floppy, Intermediate, Standard, and Extra Support. A polymer sleeve, extending from the spring coil to the proximal fluorinated polymer coated core wire, surrounds the tapered core wire and is coated with ICE™ Hydrophilic Coating. The available lengths for the guide wires will be ChoICE-190 cm, ChoICE Plus-182 cm and ChoICE Exchange-300 centimeters.
IV. Intended Use:
The SCIMED ChoICE™ Guide Wires are intended to facilitate the placement and exchange of balloon dilatation catherers or other therapeutic devices
during PTCA or other intravascular interventional procedures. The ChoICE™ Guide Wire family is not intended for use in the cerebral vasculature. The devices are provided sterile and intended for one procedure only.
Corporate Headquarters One SCIMED Place Maple Grove, MN 55311-1566 USA 612-494-1700
1
510(K) Notification SCIMED ChoICE, ChoICE Plus, ChoICE Exchange PTCA Guide Wires Page 4
Summary of Technological Characteristics: V.
The modified ChoICE, ChoICE Plus, and ChoICE Exchange PTCA Guide Wires utilize the same materials and methods of construction as the currently marketed ChoICE, ChoICE Plus, and ChoICE Exchange PTCA Guide Wires. The modifications consist of a formulation change to the distal polyurethane material, and an alternative manufacturing method for attaching the proximal end of the spring coil.
VI. Non-Clinical Test Summary:
Testing and evaluation of the guide wires included ICE lubricious coating adherence, polyurethane shear strength, polyurethane adherence, and proximal spring coil joint shear testing. In addition, shelf life testing was performed on test units with the modified polyurethane material. Test results verified that the modified ChoICE, ChoICE Plus, and ChoICE Exchange met the design requirements and are adequate for their intended use. The modified ChoICE, ChoICE Plus, and ChoICE Exchange are considered to be substantially equivalent to the ChoICE, ChoICE Plus, and ChoICE Exchange guide wires currently marketed by SCIMED, based on a comparison of intended use, design and the results of in vitro testing and evaluation. Torque testing also parformal .
SYSTEMS, INC.