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Non absorbable Surgical Polypropylene Suture is indicated for use in general soft tissue approximation and/or ligation, but not for use in ophthalmic procedures, cardiovascular and neurological procedures. The device is limited to use where short term wound support (7-10 days) is required and can be left in place for a maximum of 10 days.

Device Description

The subject device is a nonabsorbable monofilament surgical suture which is supplied sterile. The proposed device is dyed blue. The color additive is [phtalocyaninato(2-)] copper(Color Index Number 74160), and the weight percentage for the color additive is less than 0.1%. The device will be offered in diameters ranging from USP size 6-0 through 2 and is available in length 75cm or 150cm with or without needles attached. Polypropylene suture meets all the requirements of USP for Non-absorbable surgical suture.

AI/ML Overview

The provided text describes the 510(k) summary for a Non Absorbable Surgical Polypropylene Suture (K230746). It focuses on demonstrating substantial equivalence to a predicate device (K080684) through non-clinical performance data.

Here's a breakdown of the requested information based on the provided document:

1. Table of acceptance criteria and the reported device performance

The document does not explicitly provide a single table listing "acceptance criteria" alongside "reported device performance" in a quantitative manner for most tests. Instead, it lists the standards the device complies with for various performance aspects and states that the test results met these requirements.

However, some specific acceptance criteria and general performance statements are given:

Criterion Type	Acceptance Criteria	Reported Device Performance
Diameter of suture	Comply with USP	"the test result shows that the length and diameter of the proposed device met the acceptance criteria." (General statement, implies compliance with USP )
Needle Attachment	Comply with USP	Reported as "Same" as predicate, implying compliance with USP
Tensile Strength	Comply with USP	Implied compliance with USP
Length	Not less than 95.0% of the length stated on the label	"the test result shows that the length and diameter of the proposed device met the acceptance criteria." (General statement, implies compliance with this criterion)
Cytotoxicity	The viability is not reduced to less than 70%	The device passed, implying viability was not reduced to less than 70%
Sensitization	The Magnusson and Kligman grades is less than 1.	The device passed, implying grades less than 1.
Intracutaneous Reactivity	The erythema and edema grades is less than 1.0.	The device passed, implying grades less than 1.0.
Acute systemic toxicity	No animal died or abnormal behavior occurred.	The device passed, implying no animal died or abnormal behavior occurred.
Pyrogen	Temperature raise is less than 0.5℃ No behavioral change or sign of toxicity was observed. Clinical pathology parameter within the reference range.	The device passed, implying these conditions were met.
Subacute Systemic Toxicity	No macroscopic changes in the viscera at necropsy. Histopathology within normal histomorphological limits	The device passed, implying these conditions were met.
Bacterial Reverse Mutation	No obviously increase in the mean number of revertant of colonies between the test group and control group.	The device passed, implying no obvious increase.
Chromosome Aberration	No significant difference in the percentage of cells with chromosome aberrations between the test group and control group.	The device passed, implying no significant difference.
Gene Mutation	There was no significant difference in the TFT-resistant mutant frequency between the test article	The device passed, implying no significant difference.
Implantation	No lesion at the implantation site. The irritation score is less than 1.0.	The device passed, implying no lesion and irritation score less than 1.0.
Hemolysis	Hemolytic index is less than 2%	The device passed, implying hemolytic index less than 2%.
Seal Strength	Complies with ASTM F88/F88M-15	"The test results demonstrated that the subject device complies with the following standards" (including ASTM F88/F88M-15).
Detecting Seal Leaks	Complies with ASTM F1929-15	"The test results demonstrated that the subject device complies with the following standards" (including ASTM F1929-15).
Hemolytic Properties	Complies with ASTM F756-17	"The test results demonstrated that the subject device complies with the following standards" (including ASTM F756-17).
EO Sterilization Residuals	Complies with ISO 10993-7:2008	"The test results demonstrated that the subject device complies with the following standards" (including ISO 10993-7:2008).
Penetration Testing of Needles	Complies with ASTM F3014-14	"The test results demonstrated that the subject device complies with the following standards" (including ASTM F3014-14).
Bend Testing of Needles	Complies with ASTM F1874-98	"The test results demonstrated that the subject device complies with the following standards" (including ASTM F1874-98).

2. Sample size used for the test set and the data provenance

The document does not specify the sample sizes for any of the non-clinical tests mentioned.
The data provenance is also not specified, as these are bench tests and biological evaluations, not human data. It is implied these tests were conducted by the manufacturer or a contracted lab to meet international standards.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

This question is not applicable to the provided information. The tests conducted are non-clinical (bench testing, biocompatibility). There is no "test set" requiring expert ground truth establishment in the context of diagnostic performance or clinical outcomes. The "ground truth" for these tests comes from adherence to established scientific and regulatory standards (e.g., USP, ISO, ASTM).

4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

This question is not applicable. Adjudication methods like 2+1 or 3+1 are used in clinical studies or diagnostic performance evaluations involving human interpretation. The reported tests are non-clinical lab tests and biocompatibility assessments, where results are typically objective measurements or observations against predefined criteria.

5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

This question is not applicable. The device is a surgical suture, not an AI-powered diagnostic tool. No MRMC study or AI assistance is mentioned or relevant to this device.

6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done

This question is not applicable. The device is a surgical suture, not an algorithm or AI system.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

The "ground truth" for the non-clinical tests is established by adherence to recognized international standards and pharmacopeial monographs. For example:

**USP , , **: These are pharmacopeial standards defining requirements for suture diameter, needle attachment, and tensile strength.
ISO 10993 series: These are international standards for the biological evaluation of medical devices, covering aspects like cytotoxicity, sensitization, systemic toxicity, genotoxicity, implantation, and hemolysis.
ASTM standards: These are industrial standards covering material properties and packaging (e.g., seal strength, dye penetration, needle bend/penetration).

The ground truth is based on the objective criteria and methodologies outlined in these standards.

8. The sample size for the training set

This question is not applicable. There is no "training set" as this is not a machine learning or AI device. The submission focuses on verifying the physical and biological characteristics of a mechanical device against established standards.

9. How the ground truth for the training set was established

This question is not applicable, as there is no training set for this device.

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