(292 days)
Not Found
No
The device description focuses on the mechanical reprocessing of a physical surgical instrument and does not mention any software, algorithms, or data processing that would indicate the use of AI/ML.
No.
The device is described as an instrument intended to pass sutures through soft tissue during surgery, which is a surgical tool, not a therapeutic device designed to cure, mitigate, treat, or prevent disease.
No
The device is intended to pass sutures through soft tissue during surgery, which is a therapeutic rather than a diagnostic function.
No
The device description clearly details physical components made of stainless steel and polycarbonate, and the reprocessing process involves cleaning, testing, and sterilization of these physical devices. There is no mention of software as the primary or sole component.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is to "pass sutures through soft tissue during endoscopic/laparoscopic surgery." This is a surgical procedure performed on the patient's body, not a test performed on a sample taken from the body.
- Device Description: The description details a mechanical instrument used for manipulating tissue and sutures during surgery. It does not describe a device used to analyze biological samples (like blood, urine, tissue biopsies, etc.) to diagnose a condition or provide information about a patient's health status.
- Lack of IVD Characteristics: The text does not mention any of the typical characteristics of an IVD, such as:
- Analyzing biological samples.
- Providing diagnostic information.
- Using reagents or assays.
- Measuring biomarkers or analytes.
The device is a surgical instrument used for a procedural purpose, not a diagnostic purpose.
N/A
Intended Use / Indications for Use
Reprocessed Suture Passers are intended to pass sutures through soft tissue during endoscopic/laparoscopic surgery.
Product codes (comma separated list FDA assigned to the subject device)
NLM
Device Description
The Reprocessed Suture Passer is a set of previously used devices that have been cleaned, tested, inspected, marked with an identifier, packaged, labeled, and sterilized by Vanguard. A "Suture Passer" is a set of three (3) devices, consisting of one (1) Carter-Thomason needle-point suture passer and two (2) suture passer guides. The Carter-Thomason needle-point suture passer is a 3mm diameter stainless steel shaft with a polycarbonate ring-grip handle that opens one side of the pointed tip of the steel shaft when activated. The polycarbonate suture passer guides have a cylindrical hub at the proximal end and a tapered shaft at the distal end. The suture passer guides taper from the junction with the cylindrical hub to the tip. Each suture passer guide has two holes in the hub; the two holes open on opposite sides of the pilot guide shaft. A Suture Passer Guide is inserted into the wound site. A Suture Passer is used to push suture through the suture passer guide and then through the tissue of the wound site. The suture is then retrieved and pulled through the opposite side of the guide. This creates a "loop" that encompasses the full depth of the wound and upon removal of the guide allows full closure of the wound. Vanguard receives previously used Suture Passers from healthcare facilities; cleans, inspects, tests, packages, labels, and sterilizes the devices; and returns them to a healthcare facility for subsequent use. The Vanguard Reprocessed Suture Passers are essentially identical to the currently marketed Original Equipment Manufacturer (OEM) devices. Device materials, specifications, and technological characteristics are equivalent. Cleaning, sterilization, and packaging validations, and performance and biocompatibility testing demonstrate that the reprocessed devices perform as intended and are safe and effective.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
soft tissue
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)
Cleaning, sterilization, and packaging validations, and performance and biocompatibility testing demonstrate that the reprocessed devices perform as intended and are safe and effective.
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.
Not Found
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
§ 876.1500 Endoscope and accessories.
(a)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.(b)
Classification —(1)Class II (special controls). The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.
0
510(k) Summary of Safety & Effectiveness
Kos 3585
| Submitter | Vanguard Medical Concepts, Inc. 5307 Great Oak Drive Lakeland, FL 33815 |
|---|---|
| Contact | Trish Stephens R&D Project Manager 863-683-8680 x252 [voice] 863-904-1604 [facsimile] tstephens@safe-reuse [email] |
| Date | December 22, 2005 |
| Device | Trade Name: Vanguard Reprocessed Suture PasserCommon Name: Suture Passer, Carter-Thomason Needle-Point Suture Passer Classification Name: Laparoscope, General & Plastic Surgery, Reprocessed 21 CFR Section: 876.1500Reprocessed - Class IIProduct Code: NLM |
| Predicate Devices | Trade Names: Inlet Medical, Inc. CloseSure® Procedure Kit510(k) numbers: K980123: Louisville Laboratories, Inc. (Inlet Medical, Inc.) Carter-Thomason Needle-Point Suture Passer Instrument Kit |
| Indications for Use | Reprocessed Suture Passers are intended to pass sutures through soft tissue during endoscopic/laparoscopic surgery. |
OCT 11 2006Continued on next page
1
510(k) Summary of Safety & Effectiveness, Continued
The Reprocessed Suture Passer is a set of previously used devices that have Device been cleaned, tested, inspected, marked with an identifier, packaged, labeled, Description and sterilized by Vanguard. A "Suture Passer" is a set of three (3) devices, consisting of one (1) Carter-Thomason needle-point suture passer and two (2) suture passer guides. The Carter-Thomason needle-point suture passer is a 3mm diameter stainless steel shaft with a polycarbonate ring-grip handle that opens one side of the pointed tip of the steel shaft when activated. The polycarbonate suture passer guides have a cylindrical hub at the proximal end and a tapered shaft at the distal end. The suture passer guides taper from the junction with the cylindrical hub to the tip. Each suture passer guide has two holes in the hub; the two holes open on opposite sides of the pilot guide shaft. A Suture Passer Guide is inserted into the wound site. A Suture Passer is used to push suture through the suture passer guide and then through the tissue of the wound site. The suture is then retrieved and pulled through the opposite side of the guide. This creates a "loop" that encompasses the full depth of the wound and upon removal of the guide allows full closure of the wound. Vanguard receives previously used Suture Passers from healthcare facilities; cleans, inspects, tests, packages, labels, and sterilizes the devices; and returns them to a healthcare facility for subsequent use. The Vanguard Reprocessed Suture Passers are essentially identical to the Technological currently marketed Original Equipment Manufacturer (OEM) devices. Characteristics Device materials, specifications, and technological characteristics are equivalent. Cleaning, sterilization, and packaging validations, and performance and Test Data biocompatibility testing demonstrate that the reprocessed devices perform as intended and are safe and effective. Based upon the information provided herein and the 510(k) "Substantial Conclusion Equivalence" Decision Making Process Chart, we conclude that Vanguard Reprocessed Suture Passers are substantially equivalent to their predicate devices under the Federal Food, Drug and Cosmetic Act.
2
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH AND HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized symbol that resembles three human profiles facing to the right, connected by flowing lines.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 1 1 2006
Ascent Healthcare Solutions % Ms. Moira Barton Regulatory Affairs Manager 10232 South 51st Street Phoenix, Arizona 85044
Re: K053585 - Supplemental Validation Submission Trade/Device Name: See Enclosed List Regulation Number: 21 CFR 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: II Product Code: NLM Dated: January 12, 1998 Received: January 14, 1998
Dear Ms. Barton:
The above-referenced premarket notification (510(k)) was cleared by the Office of Device Evaluation (ODE) on March 9, 1998. We have received your supplemental validation data as required for reprocessed single-use devices by the Medical Device User Fee and Modernization Act of 2002. After reviewing your supplemental validation data, we have determined the devices listed in the enclosure accompanying this letter are 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 these devices, 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.
If your devices are classified (see above) into either class II (Special Controls) or class III (PMA) they may be subject to such 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 devices 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 devices comply 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 applicable requirements, including, but not limited to: registration and
3
Page 2 -- Ms. Moira Barton
listing (21 CFR Part 807); labeling (21 CFR Part 801); 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.
The FDA finding of substantial equivalence of your devices to legally marketed predicate devices results in classification for your devices and thus, permits you to legally market the devices. This letter will allow you to continue marketing the devices listed in the enclosure accompanying this letter.
If you desire specific advice for your devices on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at 240-276-0115. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html.
Sincerely yours,
Va. Mcllroy
Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
Page 4 - Ms. Moira Barton
Device listing found to be substantially equivalent:
Carter-Thomason CloseSure System
- (1) Carter-Thomason Need-Point Suture Passer
.
,
.
1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 - 1999 -
- (1) 5mm Suture Passer
.
.
:
- (1) 10/12mm Suture Passer Guide
5
Indications for Use
510(k) Number (if known):
Device Name: Vanguard Reprocessed Suture Passers
Indications for Use:
Reprocessed Suture Passers are intended to pass sutures through soft tissue during endoscopic/laparoscopic surgery.
| Prescription Use | X |
|---|---|
| (Part 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)
(Division Sign-Off) Division of General, Restorative, and Neurological Devices
Page 1 of 1
510(k) Number / K053585
012