(89 days)
Not Found
Not Found
No
The device description and performance studies focus on the mechanical properties and function of a suture clip and handle, with no mention of software, algorithms, or data processing that would indicate AI/ML.
No
The device is described as a "suture clip" used for "general soft tissue approximation and /or ligation." It is a mechanical device for holding tissues together, not for treating a disease or condition itself.
No
The device is described as a "suture clip" used for "general soft tissue approximation and/or ligation," which are mechanical functions for surgical repair, not for gathering or interpreting data about a patient's health status.
No
The device description clearly outlines multiple physical components made of materials like acetal, polysulfone, and stainless steel, which are assembled into a Y-Knot assembly and a handle. This indicates a hardware-based medical device, not a software-only one.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is "for use in general soft tissue approximation and /or ligation with #1 and #2 braided polyester suture." This describes a surgical procedure performed on the body, not a test performed on a sample taken from the body.
- Device Description: The description details a mechanical device used to secure sutures during surgery. It does not mention any components or processes related to analyzing biological samples (like blood, urine, tissue, etc.).
- Lack of IVD Characteristics: There is no mention of analyzing samples, detecting substances, diagnosing conditions based on sample analysis, or any other typical function of an IVD.
Therefore, the Innovasive Y-Knot Suture Clip is a surgical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The Intended Use for the Innovasive Y-Knot Suture Clip is for use in general soft tissue approximation and /or ligation with #1 and #2 braided polyester suture.
Product codes (comma separated list FDA assigned to the subject device)
79 FZP, KOG
Device Description
The device consists of two distinct assemblies, both of which are required to properly deploy and use the device. These assemblies are the Y-Knot assembly and the handle.
Y-Knot assembly: The shaft portion of the assembly consists of the connector, outer tube, pull rod, shaft tube end, adapter, spring pin and dowel pin. These components are used to support the implant portion of the device and aid in the deployment of the Y-Knot when ready for use. The materials for each of these components are listed on each drawing. The shaft assembly is also fitted with two threaders. This allows the Y-Knot to be threaded with the suture when ready for use. The threaders pass through the inner member of the Y-Knot. When suture is passed through the loop of the threader, the threader is withdrawn. This results in the suture passing through and exiting the inner member. The threader is then discarded.
The implant portion consists of two components, the Y-Knot inner member and the sleeve. The inner member is molded of acetal. The sleeve portion of the device consists of machined acetal.
Handle: The handle will be offered as a reusable component. The handle is a device intended to be connected to the Y-Knot assembly connector and is used to deploy the device. The handle will be offered in two versions. One will be a limited reusable plastic handle constructed of Radel polysulfone material and a stainless steel locking mechanism. A second version, will be an all stainless steel reusable handle for long term reuse.
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)
The following performance data was provided in support of the substantial equivalence determination:
- Static Strength: The strength of Y-Knot suture fixation with #1 and #2 polyester suture was compared to the same suture utilizing knots and were found to be equivalent.
- Fatigue Strength: The strength of the Y-Knot compared to the suture with knots was tested at 80% and 60% loads to compare their fatigue characteristics. They were found to be equivalent.
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.
Not Found
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
K973313
DEC - 1 1997
510(K) SUMMARY
1. SUBMITTER:
Innovasive Devices, Inc. 734 Forest St. Marlborough, MA 01752 Telephone: 508-460-8229
Contact: Eric Bannon, Vice President of Quality Assurance and Regulatory Affairs Date Prepared: August 26, 1996
2. DEVICE:
Trade Name: Innovasive Devices Y-Knot Suture Clip Classification Name: Implantable Clip The Product Code is 79 FZP
3. PREDICATE DEVIČE:
The predicate device used to determine substantial equivalence for the Innovasive Devices Y-Knot Suture Clip was Ethibond Extra polyester suture produced by Ethicon, Inc., Somerville, N.J.
4. DEVICE DESCRIPTIONS:
The device consists of two distinct assemblies, both of which are required to properly deploy and use the device. These assemblies are the Y-Knot assembly and the handle.
Y-Knot assembly: The shaft portion of the assembly consists of the connector, outer tube, pull rod, shaft tube end, adapter, spring pin and dowel pin. These components are used to support the implant portion of the device and aid in the deployment of the Y-Knot when ready for use. The materials for each of these components are listed on each drawing. The shaft assembly is also fitted with two threaders. This allows the Y-Knot to be threaded with the suture when ready for use. The threaders pass through the inner member of the Y-Knot. When suture is passed through the loop of the threader, the threader is withdrawn. This results in the suture passing through and exiting the inner member. The threader is then discarded.
The implant portion consists of two components, the Y-Knot inner member and the sleeve. The inner member is molded of acetal. The sleeve portion of the device consists of machined acetal.
000165
1
Handle: The handle will be offered as a reusable component. The handle is a device intended to be connected to the Y-Knot assembly connector and is used to deploy the device. The handle will be offered in two versions. One will be a limited reusable plastic handle constructed of Radel polysulfone material and a stainless steel locking mechanism. A second version, will be an all stainless steel reusable handle for long term reuse.
5. INTENDED USE:
The Intended Use for the Innovasive Y-Knot Suture Clip is for use in general soft tissue approximation and /or ligation.
6. COMPARISON OF CHARACTERISTICS:
The Y-Knot suture clip consists of acetal plastic compared to the polyester material of the Ethicon Ethibond Suture.
The Y-Knot uses a mechanical means through the use of mating parts to secure two ends of a suture. This fixation essentially replaces the knot component of the suture. Suture utilizes a knot as the primary fixation method.
The indications for use for both products are identical.
7. PERFORMANCE DATA:
The following performance data was provided in support of the substantial equivalence determination:
-
- Static Strength: The strength of Y-Knot suture fixation with #1 and #2 polyester suture was compared to the same suture utilizing knots and were found to be equivalent.
-
- Fatigue Strength: The strength of the Y-Knot compared to the suture with knots was tested at 80% and 60% loads to compare their fatigue characteristics. They were found to be equivalent.
000106
2
sleeve component at the distal portion of the Y-Knot to move towards, and make contact with, the inner member to which the suture has been passed. As the sleeve mates with the inner member, the suture is captured between the two components. The sleeve then locks onto the locking ring of the inner member. This action of the sleeve mating with the inner member results in the suture not only being secured, but tightened as well. The tightening is due to the suture being drawn up slightly as the sleeve and inner member components mate. As the stroke of the trigger is completed, the inner member pull through component is sheared just above the mating location of the device. The device is now completely deployed resulting in both ends of the suture strand being secured with the Y-Knot Suture Clip. The remaining portion of the device not affixed to the suture is now discarded.
VIII. PACKAGING
The Y-Knot will be packaged in a double protective sterile barrier configuration. The blister will consist of a formed PETG blister or similar material. The lid sealed to the blister will consist of Tyvek 1073B. This package will then be sealed in a chevron pouch. The pouch will consist of mylar laminated to 1073B Tyvek. The blister as well as the pouch will be labeled with the information contained in the labeling section of this submission.
Drawings of the proposed packaging configuration are found in Attachment 7.
STERILIZATION IX.
The method of sterilization for the proposed Y-Knot Suture Clip will be either Ethylene Oxide gas or Gamma Radiation. Each method is summarized below:
- Ethylene Oxide Gas: The sterility assurance level for this method will 10th. The A: sterilization will be completed by a contract facility. The process will be validated per ANSI/AAMI/ISO 11135 - 1994 Half Cycle Method. The ETO residual levels will be 250, 250 and 5000 ppm for Ethylene Oxide, Ethylene Chlorhydrin and Ethylene Gycol, respectively. The Suture Fastener will continue to be labeled as non-pyrogenic. The LAL method will be used.
- Gamma Radiation: The sterility assurance level for this method will be 10 . The B: sterilization will be completed by a contract facility. The process will be validated per ANSI/AAMI/ISO 11137. The minimum acceptable dose for dosimetric release will be 2.5 Mrad, the maximum dose will be 5.0 Mrad. The Suture Fastener will continue to be labeled as non-pyrogenic. The LAL method will be used.
X. LABELING
The Instructions For Use and proposed labeling for the fastener are found in Attachment 8. The labels for the individual sterile fasteners are included as well. These labels are
3
Image /page/3/Picture/1 description: The image is a black and white seal for the U.S. Department of Health & Human Services. The seal is circular, with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the top half of the circle. The bottom half of the circle contains a stylized image of an eagle with its wings spread.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Mr. Eric Bannon 'Vice President of Regulatory Affairs and Quality Assurance Innovasive® Devices 734 Forest Street Marlborough, Massachusetts 01752
DEC - 1 1997
Re: K973313
Trade Name: Innovasive Devices Y-Knot Suture Clip Regulatory Class: II Product Code: KOG Dated: September 2, 1997 Received: September 3, 1997
Dear Mr. Bannon:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). 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.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it 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 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirements , as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (OS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
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Page 2 - Mr. Eric Bannon
This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4595. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours,
Ascollars
Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
INDICATIONS FOR USE
The Intended Use for the Innovasive Y-Knot Suture Clip is for use in general soft tissue approximation and /or ligation with #1 and #2 braided polyester suture.
Prescription Use
(Per 21 CFR 801.109)
coo
(Division Sign-Off) Division of General Restorati 510(k) Number