(454 days)
The Captix Foreign Body Retriever is indicated for use in the retrieval of foreign bodies misplaced during interventional radiological procedures in the neuro, peripheral and coronary vasculature.
Like the predicate device, the Captix Retriever consists of a flexible, tapered core wire with a shaped section at the distal end. A platinum coil at the distal end allows fluoroscopic visualization. Retriever dimensions are indicated on the product label. The Retriever has a hydrophilic coating to reduce friction during use. A torque device and an insertion tool are provided with the Retriever.
I am sorry, but the provided text does not contain the specific information required to complete your request. The document is a 510(k) summary for a medical device (Captix™ Retriever) and describes its intended use, predicate device, materials, and a general summary of verification and validation testing.
However, it does not provide:
- A table of acceptance criteria and reported device performance with specific metrics.
- Sample sizes for test sets, data provenance, or details on ground truth establishment (experts, adjudication methods).
- Information on multi-reader multi-case (MRMC) studies or standalone algorithm performance.
- Sample size or ground truth details for a training set, as this is not an AI/ML device.
The "Testing Summary" section broadly states that the device conforms to pre-determined specifications and confirms substantial equivalence to a predicate device, but it lacks the detailed quantitative information you've requested regarding acceptance criteria and performance against those criteria. The tests mentioned (e.g., kink resistance, tensile, radiopacity, retrievability, in-vivo animal testing) are general categories of engineering and biological performance, not specific acceptance criteria in the format you've outlined.
Therefore, I cannot provide the requested table and detailed study information based on the given text.
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KO93610
510(k) SUMMARY OF SAFETY AND EFFECTIVENESS
General Information
FEB 1 7 2011
| Trade Name | Captix™ Retriever |
|---|---|
| Common Name | Endovascular Retriever |
| Classification | Percutaneous Catheter, 21CFR 870.1250 – Class II |
| Submitter | Concentric® Medical, Inc.301 E. Evelyn AvenueMountain View, CA 94041Tel 650-938-2100Fax 650-237-5230 |
| Contact | Kirsten ValleySenior Vice President, Technology and Regulatory Affairs |
Intended Use
The intended use for the Captix Retriever is the same as the intended use for the predicate Retriever:
The Captix Retriever is indicated for use in the retrieval of foreign bodies misplaced during interventional radiological procedures in the neuro, peripheral and coronary vasculature.
Predicate Device
K030476 - Modified Concentric Retriever Model 90037
Device Description
Like the predicate device, the Captix Retriever consists of a flexible, tapered core wire with a shaped section at the distal end. A platinum coil at the distal end allows fluoroscopic visualization. Retriever dimensions are indicated on the product label. The Retriever has a hydrophilic coating to reduce friction during use. A torque device and an insertion tool are provided with the Retriever.
Materials
The materials used in the Captix Retriever are the same as the materials used in the predicate device.
All materials used in the manufacture of the Captix Retriever are suitable for the intended use of the device and have been used in numerous previously cleared products.
DCC
2.16.11
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Testing Summary
Results of design verification and validation testing performed on the Captix Retriever confirm that the device conforms to the pre-determined specifications. The test results were comparable to those of the predicate Concentric Medical foreign body retriever establishing substantial equivalence to the predicate device.
- Simulated anatomy/concomitant device use the device was evaluated in a simulated anatomy . model and the following were assessed: catheter compatibility, deliverability and deployment, and accessory compatibility.
- Kink resistance the device's resistance to kinking was evaluated in simulated anatomy 앞 demonstrating that the device appropriately resisted kinking under simulated use conditions.
- Torque/tensile the device's ability to withstand torque and tensile loads was evaluated . demonstrating the device's mechanical strength and durability for the specified number of retrieval attempts.
- Radiopacity the visibility of the device under fluoroscopy was evaluated demonstrating the . device's ability to be seen during clinical procedures.
- Tensile the tensile strength of the device was determined demonstrating the device's . mechanical integrity.
- Retrievability the ability of the device to retrieve foreign bodies in a simulated anatomy model . was evaluated and demonstrated that the device meets the user needs without loss of mechanical integrity.
- ♥ In-vivo animal testing - simulated use testing was performed in an animal model demonstrating that the device meets the user needs and is atraumatic to the blood vessel.
Summary of Substantial Equivalence
The Captix Retriever is substantially equivalent to the predicate device with regard to intended use, operating principal, design concept, materials, shelf life, packaging and sterilization processes.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" around the perimeter. Inside the circle is a stylized symbol that resembles three overlapping lines or curves, creating a visual representation of a person with outstretched arms.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring. MD 20993-0002
Concentric Medical, Inc. c/o Ms. Kirsten Vallev Senior Vice President, Technology and Regulatory Affairs 301 East Evelyn Avenue Mountain View, CA 94041
Re: K093610
Trade/Device Name: Captix® Retriever Regulation Number: 21 CFR 870.1250 Regulation Name: Percutaneous Catheter Regulatory Class: Class II Product Code: NRY Dated: January 25, 2011 Received: January 27, 2011
FEB 1 7 2011
Dear Ms. Valley:
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 misJeading.
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.
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Page 2 - Ms. Kirsten Vallev
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-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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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 Small Manufacturers, International and Consumer Assistance 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 vours.
M.B. Egleston, Mrs
Malvina B. Eydelman, M.D. Director Division of Ophthalmic, Neurological, and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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INDICATIONS FOR USE
| 510(k) Number (if known): | K093610 |
|---|---|
| Device Name: | Captix™ Foreign Body Retriever |
| Indications for Use: | The Captix Foreign Body Retriever is indicated for use in theretrieval of foreign bodies misplaced during interventionalradiological procedures in the neuro, peripheral and coronaryvasculature. |
Prescription Use __X (Per 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH , Office of Device Evaluation (ODE)
Joe HUTTER
(Division Sign-Off) Division of Ophthalmic, Neurological and Ear, Nose and Throat Devices
510(k) Number K093610
§ 870.1250 Percutaneous catheter.
(a)
Identification. A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.(b)
Classification. Class II (performance standards).