VIDAS LYME IGM
Device Facts
| Record ID | K122979 |
|---|---|
| Device Name | VIDAS LYME IGM |
| Applicant | Biomerieux S.A. |
| Product Code | LSR · Microbiology |
| Decision Date | Jun 4, 2013 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 866.3830 |
| Device Class | Class 2 |
| Attributes | Real-World Evidence |
Real-World Evidence
| Submission | Device | Sponsor | RWD Sources | RWE Use Summary | Key Tags |
|---|---|---|---|---|---|
| K122979 · Jun 4, 2013 | VIDAS LYME IGM | Biomerieux S.A. | Retrospective clinical patient samples; Prospective clinical routine-testing samples; CDC-characterized serum panel | Retrospective and prospective clinical samples were used to evaluate clinical sensitivity, analytical specificity, and method comparison against a predicate device in routine clinical settings. | Retrospective clinical cohort; Prospective clinical study; Routine clinical testing; Clinical sensitivity; Analytical specificity |
Clinical Evidence
| Study Design | Population | Comparator | Key Endpoints |
|---|---|---|---|
| Retrospective study | 202 patients meeting a case definition of Lyme disease; Sample Size: 202 | Predicate Lyme IgM assay | Clinical sensitivity |
| Prospective study | 975 fresh or frozen prospectively collected sera submitted for routine Lyme disease testing; Sample Size: 975; Number of Sites: 3 | Predicate Lyme IgM assay | Positive Percent Agreement (PPA), Negative Percent Agreement (NPA) |
Indications for Use
The VIDAS Lyme IgM (LYM) assay is an automated qualitative enzyme immunoassay intended for use on the instruments of the VIDAS family in the presumptive detection of human IgM antibodies to Borrelia burgdorferi in human serum (plain or separation gel) or plasma (sodium heparin or lithium heparin). It should be used to test patients with a history and/or symptoms of infection with B. burgdorferi. All VIDAS Lyme IgM positive and equivocal specimens should be further tested with a Western Blot IgM assay to obtain supportive evidence of infection with B. burgdorferi.
Device Story
Automated qualitative enzyme-linked fluorescent assay (ELFA) for detection of IgM antibodies to B. burgdorferi. Input: human serum or plasma. Process: 2-step sandwich immunoassay using recombinant B. burgdorferi proteins coated on Solid Phase Receptacle (SPR); alkaline phosphatase-conjugated anti-human IgM; substrate (4-Methyl-umbelliferyl phosphate) hydrolysis produces fluorescent signal measured at 450 nm. Output: automated test value/index. Used in clinical laboratories on VIDAS/miniVIDAS instruments. Results assist clinicians in identifying potential Lyme disease, requiring follow-up with Western Blot for confirmation.
Clinical Evidence
Prospective study (n=975) compared VIDAS Lyme IgM to predicate EIA. 1st-tier PPA 51.0% (95% CI 44.0-57.9%). 2nd-tier PPA (vs Western Blot) 80.8% (95% CI 72.2-87.2%). Retrospective sensitivity study (n=202) showed 66.8% overall sensitivity. Analytical specificity evaluated in 200 healthy subjects (13% positive/equivocal). Cross-reactivity tested against 19 conditions; highest cross-reactivity observed with HIV (35.0%), CMV (17.6%), and HSV (15.3%).
Technological Characteristics
Automated ELFA using Solid Phase Receptacle (SPR) technology. Reagents: recombinant B. burgdorferi proteins, alkaline phosphatase conjugate, 4-Methyl-umbelliferyl phosphate substrate. Detection: fluorescence at 450 nm. Sample types: serum (plain/gel), plasma (sodium/lithium heparin). Instrument: VIDAS/miniVIDAS family. Software: automated calculation of test index.
Indications for Use
Indicated for presumptive detection of human IgM antibodies to Borrelia burgdorferi in human serum or plasma. Target population: patients with history or symptoms of B. burgdorferi infection. Positive/equivocal results require follow-up with Western Blot IgM assay.
Regulatory Classification
Identification
Treponema pallidum treponemal test reagents are devices that consist of the antigens, antisera and all control reagents (standardized reagents with which test results are compared) which are derived from treponemal sources and that are used in the fluorescent treponemal antibody absorption test (FTA-ABS), the Treponema pallidum immobilization test (T.P.I.), and other treponemal tests used to identify antibodies to Treponema pallidum directly from infecting treponemal organisms in serum. The identification aids in the diagnosis of syphilis caused by bacteria belonging to the genus Treponema and provides epidemiological information on syphilis.
Predicate Devices
- Platelia™ Lyme IgM (K081362)
Submission Summary (Full Text)
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# 510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY
A. 510(k) Number: K122979
B. Purpose for Submission: New device
C. Measurand: IgM antibodies to *Borrelia burgdorferi* proteins
D. Type of Test: Enzyme immunoassay
E. Applicant: bioMerieux SA
F. Proprietary and Established Names: VIDAS® Lyme IgM
## G. Regulatory Information:
1. Regulation section: 21 CFR 866.3830; Treponema pallidum treponemal test reagents
2. Classification: Class II
3. Product code: LSR; Reagent, Borrelia Serological Reagent
4. Panel: Microbiology
## H. Intended Use:
1. Intended use(s): The VIDAS Lyme IgM (LYM) assay is an automated qualitative enzyme immunoassay intended for use on the instruments of the VIDAS family in the presumptive detection of human IgM antibodies to *Borrelia burgdorferi* in human serum (plain or separation gel) or plasma (sodium heparin or lithium heparin). It should be used to test patients with a history and/or symptoms of infection with *B. burgdorferi*. All VIDAS Lyme IgM positive and equivocal specimens should be further tested with a Western Blot IgM assay to obtain supportive evidence of infection with *B. burgdorferi*.
2. Indication(s) for use: The VIDAS Lyme IgM (LYM) assay is an automated qualitative enzyme immunoassay intended for use on the instruments of the VIDAS family in the presumptive detection of human IgM antibodies to *Borrelia burgdorferi* in human serum (plain or separation gel) or plasma (sodium heparin or lithium heparin). It should be used to test patients with a history and/or symptoms of infection with *B. burgdorferi*. All VIDAS Lyme IgM positive and equivocal specimens should be further tested with a Western Blot IgM assay to obtain supportive evidence of infection with *B. burgdorferi*.
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3. Special conditions for use statement(s): For prescription use
4. Special instrument requirements: VIDAS and miniVIDAS instruments
I. Device Description: The VIDAS Lyme IgM assay principle combines a 2-step enzyme immunoassay sandwich method with a final fluorescent detection (ELFA). The Solid Phase Receptacle (SPR®) serves as the solid phase as well as the pipetting device for the assay. Reagents for the assay are ready-to-use and predisposed in the sealed reagent strips. All of the assay steps are performed automatically by the instrument. The reaction medium is cycled in and out of the SPR several times.
After a preliminary wash step and a sample dilution step, the antibodies to B. burgdorferi present in the specimen will bind to the B. burgdorferi specific recombinant proteins coating the interior of the SPR. Unbound sample components are washed away. Anti-human IgM antibodies conjugated with alkaline phosphatase will attach to the immunocomplex bound to the SPR wall.
A final wash step removes unbound conjugate. During the final detection step, the substrate (4-Methyl-umbelliferyl phosphate) is cycled in and out of the SPR. The conjugate enzyme catalyzes the hydrolysis of this substrate into a fluorescent product (4-Methyl-umbelliferone) the fluorescence of which is measured at 450 nm. The intensity of the fluorescence is proportional to the quantity of anti-B.burgdorferi IgM antibody present in the sample.
At the end of the VIDAS Lyme IgM assay, results are automatically calculated by the instrument. A test value is generated and a report is printed.
J. Substantial Equivalence Information:
1. Predicate device name(s): Platelia™ Lyme IgM
2. Predicate 510(k) number(s): K081362
3. Comparison with predicate:
| Similarities | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Intended Use | The VIDAS Lyme IgM (LYM) assay is an automated qualitative enzyme immunoassay intended for use on the instruments of the VIDAS family in the presumptive detection of human IgM | The Platelia™ Lyme IgM Test is a qualitative test intended for use in the presumptive detection of human IgM antibodies to Borrelia burgdorferi in human serum or plasma (K3 EDTA, sodium |
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| Similarities | | |
| --- | --- | --- |
| Item | Device | Predicate |
| | antibodies to Borrelia burgdorferi in human serum (plain or separation gel) or plasma (sodium heparin or lithium heparin). It should be used to test patients with a history and/or symptoms of infection with B. burgdorferi. All VIDAS Lyme IgM positive and equivocal specimens should be further tested with a Western Blot IgM assay to obtain supportive evidence of infection with B. burgdorferi. | heparin or sodium citrate). The EIA system should be used to test serum or plasma from patients with a history and symptoms of infection with B. burgdorferi. All positive and equivocal specimens should be re- tested with a specific, second-tier test such as Western Blot. Positive second- tier results are supportive evidence of infection with B. burgdorferi. The diagnosis of Lyme disease should be made based on history and symptoms (such as erythema migrans), and other laboratory data, in addition to the presence of antibodies to B. burgdorferi. Negative results (either first or second-tier) should not be used to exclude Lyme disease. |
| Specimen | Serum or plasma | Serum or plasma |
| Analyte | IgM antibodies to Borrelia burgdorferi | IgM antibodies to Borrelia burgdorferi |
| Method | Qualitative | Qualitative |
| Differences | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Antigens | Recombinant proteins of B. burgdorferi | Whole cell extract of B. burgdorferi antigens |
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| Differences | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Assay Technique | Enzyme-linked fluorescent assay (ELFA) | Enzyme immunoassay (EIA) |
| Automated | Yes | No |
K. Standard/Guidance Document Referenced (if applicable): Not applicable
L. Test Principle: Enzyme Immunoassay
M. Performance Characteristics (if/when applicable):
1. Analytical performance:
a. Precision/Reproducibility:
Precision: For the precision study, 4 serum samples were tested in duplicate in 40 different runs (2 runs per day over 20 days) with 2 reagent lots at 1 site $(n = 80)$ . The precision was calculated following the recommendations of the CLSI® document EP5-A2. The total precision data in the table reflect the 80 values generated per sample for Site 1 and takes into account replicate, run, day, calibration, and lot as potential sources of variation. The total precision for controls includes within-day, between-days and between-calibration variability and is lot specific.
| Panel Member | N | Mean Index | Within-run | | Within-day | | Between-days | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | SD | CV (%) | SD | CV (%) | SD | CV (%) | SD | CV (%) |
| Sample 1 | 80 | 0.19 | 0.01 | 3.9 | 0.01 | 2.7 | 0.00 | 0.0 | 0.01 | 5.2 |
| Sample 2 | 80 | 0.27 | 0.01 | 4.7 | 0.01 | 2.8 | 0.00 | 1.4 | 0.02 | 9.1 |
| Sample 3 | 80 | 0.38 | 0.01 | 2.6 | 0.01 | 3.0 | 0.00 | 0.3 | 0.02 | 4.7 |
| Sample 4 | 80 | 1.31 | 0.03 | 2.1 | 0.02 | 1.6 | 0.01 | 0.9 | 0.09 | 6.9 |
| Positive Control | 40 | 0.74 | NA | NA | 0.04 | 5.3 | 0.00 | 0.0 | 0.07 | 10.1 |
| Negative Control | 40 | 0.00 | NA | NA | 0.00 | 0.0 | 0.00 | 0.0 | 0.00 | 0.0 |
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Reproducibility: For reproducibility, 4 serum samples were tested in duplicate in 40 different runs (2 runs per day over 20 days) with 2 reagent lots at 3 sites (n = 240). The reproducibility was calculated following the recommendations of the CLSI® document EP5-A2. The total reproducibility data in the table reflects the 240 values generated per sample for all sites and takes into account replicate, run, day, calibration, lot, and site as potential sources of variation. Out of the 240 total values, 2 Low Positives (Sample 3) gave an equivocal value (< 0.32). The total reproducibility for controls includes within-day, between-days, between-calibration and between-site variability and is lot specific.
| Panel Member | N | Mean Index | Within-run | | Within-day | | Between-days | | Between-site | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | SD | CV (%) | SD | CV (%) | SD | CV (%) | SD | CV (%) | SD | CV (%) |
| Sample 1 | 240 | 0.19 | 0.01 | 3.5 | 0.00 | 2.1 | 0.00 | 1.0 | 0.00 | 0.0 | 0.01 | 6.3 |
| Sample 2 | 240 | 0.26 | 0.01 | 4.3 | 0.01 | 2.7 | 0.00 | 0.7 | 0.01 | 2.1 | 0.02 | 7.8 |
| Sample 3 | 240 | 0.37 | 0.01 | 3.1 | 0.01 | 2.1 | 0.00 | 0.0 | 0.00 | 0.0 | 0.02 | 6.2 |
| Sample 4 | 240 | 1.26 | 0.03 | 2.5 | 0.02 | 1.9 | 0.01 | 0.4 | 0.00 | 0.0 | 0.12 | 9.4 |
| Positive Control | 120 | 0.72 | NA | NA | 0.03 | 4.6 | 0.00 | 0.0 | 0.00 | 0.0 | 0.09 | 12.1 |
| Negative Control | 120 | 0.00 | NA | NA | 0.00 | 0.0 | 0.00 | 0.0 | 0.00 | 0.0 | 0.00 | 0.0 |
b. Linearity/assay reportable range: N/A
c. Traceability, Stability, Expected values (controls, calibrators, or methods): N/A
d. Detection limit: N/A
e. Analytical specificity:
Testing asymptomatic population: 100 sera from apparently healthy subjects from an endemic population (New York) and 100 sera from a non-endemic population (Texas) with no known history of Lyme disease were run on the VIDAS Lyme IgM assay and the predicate Lyme IgM assay. The following results were obtained:
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| | VIDAS | | Predicate | |
| --- | --- | --- | --- | --- |
| | Positivity* | Negativity | Positivity* | Negativity |
| Endemic | 12.0% | 88.0% | 19.0% | 81.0% |
| Non-Endemic | 14.0% | 86.0% | 3.0% | 97.0% |
* Includes positives and equivocals.
Cross-reactivity: Cross-reactivity is based on the study of samples that are negative with the test being evaluated and positive for the potentially interfering disease. The results of the samples tested according to the disease are shown in the table below:
| Infection or Diagnosis | N | VIDAS Lyme IgM Equivocal or positive results | % Cross-reactivity |
| --- | --- | --- | --- |
| Anti Nuclear Antibodies | 60 | 3 | 5.00 |
| C Reactive Protein | 61 | 4 | 6.55 |
| Cytomegalovirus | 34 | 6 | 17.64 |
| Epstein Barr Virus | 65 | 7 | 10.76 |
| Helicobacter pylori | 143 | 10 | 6.99 |
| Hepatitis A Virus | 153 | 22 | 14.37 |
| Herpes Simplex Virus | 98 | 15 | 15.30 |
| Human Immunodeficiency Virus | 20 | 7 | 35.00 |
| Human Anti-mouse Antibodies | 31 | 2 | 6.45 |
| Leptospirosis | 216 | 22 | 10.18 |
| Measles | 38 | 5 | 13.15 |
| Mumps | 46 | 2 | 4.34 |
| Rheumatoid Factor | 61 | 5 | 8.19 |
| Rickettsiosis | 112 | 6 | 5.35 |
| Rubella | 19 | 2 | 10.52 |
| Syphilis | 270 | 25 | 9.25 |
| Systemic Lupus Erythematosus | 28 | 2 | 7.14 |
| Toxoplasmosis | 26 | 5 | 19.23 |
| Varicella Zoster Virus | 58 | 4 | 6.89 |
The effect of Babesiosis, Erhlichiosis and Rocky mountain spotted fever pathologies on the VIDAS Lyme IgM performance is not known.
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Interfering Substances: Interferences were studied according to the recommendations of CLSI® document EP7-A2. None of the following factors have been found to significantly influence this assay:
- hemolysis (after spiking samples with hemoglobin: 5 g/L [monomer]),
- lipemia (after spiking samples with lipids: 30 g/L equivalent in triglycerides),
- bilirubinemia (after spiking samples with bilirubin: 0.3 g/L),
- human albumin (after spiking samples with albumin up to 60 g/L).
It is recommended not to use samples that are hemolyzed, lipemic or icteric and, if possible, to collect a new sample.
f. Assay cut-off: The clinical cut-off of the assay was determined using a Receiver Operating Characteristic (ROC) curve analysis. 211 negative sera and 211 positive sera were used to determine the cut-off value that gave the best discrimination between the sensitivity and the specificity of the assay. The cut-off index value for VIDAS Lyme IgM was determined to be equal to 0.12.
## 2. Comparison studies:
a. Method comparison with predicate device:
Method Comparison: A prospective study was performed on 975 fresh or frozen prospectively collected sera submitted for routine Lyme disease testing from an endemic area of the United States. Testing was performed in three laboratories. At each laboratory, the samples were tested in parallel using a commercially available Lyme IgM EIA method (predicate) and the VIDAS Lyme IgM assay. Positive % Agreement (PPA) is calculated for the positives and equivocals together since the 2-tier testing does not make a distinction and calls for both of them to be tested by Western Blot. Combined results from the three sites are shown below:
| N = 975 | Predicate Lyme IgM | | |
| --- | --- | --- | --- |
| VIDAS Lyme IgM | Positive | Equivocal | Negative |
| Positive | 71 | 10 | 32 |
| Equivocal | 15 | 11 | 55 |
| Negative | 50 | 53 | 678 |
| Total | 136 | 74 | 765 |
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| N = 975 | Predicate Lyme IgM | | |
| --- | --- | --- | --- |
| VIDAS Lyme IgM | Positive | Equivocal | Negative |
| Positive % Agreement
95% CI | 51.0% (107/210)
[44.0 - 57.9]% | | |
| Negative % Agreement
95% CI | 88.6% (678/765)
[86.2 - 90.8]% | | |
Second-Tier Testing: In accordance with the CDC recommendations for use of a 2-tier Lyme disease testing scheme, the VIDAS Lyme IgM positive and equivocal results and the predicate Lyme IgM positive and equivocal results were confirmed using a commercially available Lyme IgM Western Blot method. The percent agreement between VIDAS and predicate Lyme IgM positives (1st tier PPA) and the percent agreement between VIDAS-predicate-Western Blot IgM positives and Predicate-Western Blot IgM positives (2nd tier PPA) are shown below.
| | 1^{st} Tier
+ or ± | IgM Western
Pos. Neg. | |
| --- | --- | --- | --- |
| Predicate IgM | 210 | 104 | 106 |
| VIDAS IgM | 194 | 95 | 93* |
| VIDAS IgM and Predicate IgM | 107 | 84 | 23 |
*, Western Blot results were not available for 6 of the positive or equivocal samples by VIDAS Lyme IgM assay.
Agreement results:
1st Tier PPA = 51.0% (107/210), 95% CI=[44.0% - 57.9%]
2nd Tier PPA= 80.8% (84/104), 95% CI=[72.2% - 87.2%]
Concordance with IgM Western Blot:
Predicate device: 49.5% (104/210)
VIDAS Lyme IgM: 49.0% (95/194)
b. Matrix comparison:
Matrix Equivalency: A matrix equivalency study for the claimed sample matrix types (serum and plasma) and tube types (a dry serum tube, a separation gel serum tube, a sodium heparinate plasma tube and a lithium heparinate plasma tube) was performed by testing thirty five samples with Index values covering the dynamic range of the assay. A 24% (2 x 12%) allowable total error was used when the VIDAS Lyme IgM index was > 0.10. At or below a 0.10 VIDAS Lyme IgM index, the allowable total error of 0.024 in terms of absolute difference was
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used. A Passing-Bablok regression was used to compare the results of each sampling tube to the results of the reference tube, the dry serum tube. For all conditions, the proportional bias was $< 12\%$ and no sample exceeded the allowable total error. The comparison study results are shown below.
Passing-Bablok regression analysis
| Tested conditions | Intercept (CI at 95%) | Slope (CI at 95%) |
| --- | --- | --- |
| Separation gel serum tube / Dry serum tube | 0.00 (-0.01 to 0.03) | 1.00 (0.93 to 1.05) |
| Lithium Heparinate plasma tube / Dry serum tube | 0.02 (-0.02 to 0.06) | 1.01 (0.91 to 1.11) |
| Sodium Heparinate plasma tube / Dry serum tube | 0.02 (-0.02 to 0.011) | 1.00 (0.77 to 1.11) |
The following table summarizes the results of the matrix equivalency study. The number and percentage $(\%)$ of specimens are reported for index differences between each sampling tube type and the reference tube.
| | Number and percentage (%) of specimens | | |
| --- | --- | --- | --- |
| Tested conditions | Index difference <10% | 10% ≤ Index difference <20% | Index difference ≥20% |
| Separation gel serum tube | 33/34 | 1/34 | 0/34 |
| | (97.0%) | (3.0%) | (0.0%) |
| Lithium Heparinate plasma tube | 26/34 | 7/34 | 1/34 |
| | (76.4%) | (20.6%) | (3.0%) |
| Sodium Heparinate plasma tube | 23/34 | 10/34 | 1/34 |
| | (67.6%) | (29.4%) | (3.0%) |
# 3. Clinical studies:
# a. Clinical Sensitivity:
Sensitivity: 202 retrospective samples from patients meeting a case definition of LD and confirmed positive for $B$ . Burgdorferi infection were run on the VIDAS Lyme IgM assay and the predicate Lyme IgM assay. For both the VIDAS Lyme IgM and the predicate test, equivocal results were considered as positive for the evaluation. The following results were obtained:
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| Stage | N | VIDAS Lyme IgM % Sensitivity * | Predicate Lyme IgM % Sensitivity * | Difference in proportions |
| --- | --- | --- | --- | --- |
| Stage I (early localized, single lesion) 1 – 30 days | 119 | 52.1 (62/119) 95% CI [42.8 – 61.3]% | 54.6 (65/119) 95% CI [45.2 - 63.8]% | -2.5% 95% CI [(-15.2)% – (10.2)%] |
| Stage II (early disseminated, multiple lesions) 1 – 30 days | 62 | 91.9 (57/62) 95% CI [82.2 - 97.3]% | 91.9 (57/62) 95% CI [82.2 – 97.3]% | 0.0% 95% CI [(-9.6)% – (9.6)%] |
| Stage III (late disseminated) | 21 | 76.2 (16/21) 95% CI [52.8 - 91.8]% | 61.9 (13/21) 95% CI [38.4 – 81.9]% | 14.3% 95% CI [(-13.3)% – (41.9)%] |
| All stages | 202 | 66.8 (135/202) 95% CI [59.9 – 73.3]% | 66.8 (135/202) 95% CI [59.9 – 73.3]% | 0.0% 95% CI [(-9.2)% – (9.2)%] |
* includes positive and equivocal results.
# b. Clinical specificity: N/A
c. Other clinical supportive data (when a. and b. are not applicable):
CDC Lyme panel: The following information is from a serum panel obtained from the CDC and tested using the VIDAS Lyme IgM kit. The results are presented as a means to convey further information on the performance of this assay with a masked, characterized serum panel. This does not imply an endorsement of the assay by the CDC.
| Time from onset | VIDAS Lyme IgM | | | Western blot IgM | | |
| --- | --- | --- | --- | --- | --- | --- |
| | Positive or equivocal | Negative | Agreement with clinical status | Positive | Negative | Agreement with clinical status |
| Normals | 1 | 4 | 80.0 % (4/5) | 0 | 5 | 100.0 % (5/5) |
| < 1 month | 3 | 2 | 60.0 % (3/5) | 3 | 2 | 60.0 % (3/5) |
| 1 – 2 months | 5 | 1 | 83.3 % (5/6) | 5 | 1 | 83.3 % (5/6) |
| 3- 12 months | 12 | 4 | 75.0 % (12/16) | 7 | 9 | 43.8 % (7/16) |
| > 1 year | 3 | 4 | 42.9 % (3/7) | 3 | 4 | 42.9 % (3/7) |
| Total | 24 | 15 | 69.2% (27/39) | 18 | 21 | 59.0 % (23/39) |
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# 5. Expected values/Reference range:
Expected values: The following tables summarize the expected (observed) values for the sensitivity, analytical specificity, and method comparison studies performed with VIDAS Lyme IgM assay.
Sensitivity study: The table below shows the results of testing with the VIDAS Lyme IgM assay (LYM) using a population of 202 patients with case-defined Lyme disease. This population was $65.3\%$ male, $34.7\%$ female with a mean age of 48 years. The VIDAS LYM test values ranged from 0.00 to 5.87 with overall positivity of $59.4\%$ . The VIDAS Lyme IgM sensitivity for stage I samples increased with increasing duration of symptoms, with a positivity rate of $38.7\%$ in the first week, but reaching $70.0\%$ by week 4 of symptoms. The positivity rate for stage II samples reached $93.8\%$ by week 2 of post-onset of symptoms. The positivity rate for stage III samples was $66.7\%$ .
LYM Values - Sensitivity Study
| Population | N | Days post- onset | Age (Mean) | % Male | % Female | Index Range | % Positive Results |
| --- | --- | --- | --- | --- | --- | --- | --- |
| Stage I: Single Lesion | 62 | 1-7 | 48 | 58.1 | 41.9 | [0.00-4.64] | 38.7 |
| | 30 | 8-14 | 51 | 60.0 | 40.0 | [0.00-5.18] | 40.0 |
| | 17 | 15-21 | 46 | 58.8 | 41.2 | [0.01-4.66] | 52.9 |
| | 10 | 22-30 | 49 | 90.0 | 10.0 | [0.09-5.06] | 70.0 |
| | 119 | Total | 49 | 61.3 | 38.7 | [0.00-5.18] | 43.7 |
| Stage II: Multiple Lesions | 29 | 1-7 | 47 | 72.4 | 27.6 | [0.03-5.77] | 82.8 |
| | 16 | 8-14 | 47 | 75.0 | 25.0 | [0.03-5.87] | 93.8 |
| | 13 | 15-21 | 46 | 69.2 | 30.8 | [0.28-5.71] | 92.3 |
| | 4 | 22-30 | 41 | 100.0 | 0.0 | [0.29-5.28] | 75.0 |
| | 62 | Total | 46 | 74.2 | 25.8 | [0.03-5.87] | 87.6 |
| Stage III: Late Disseminated | 21 | Total | 49 | 57.1 | 42.9 | [0.00-5.44] | 66.7 |
| All samples | 202 | Total | 48 | 65.3 | 34.7 | [0.00-5.87] | 59.4 |
Analytical Specificity Study: The table below shows the results of testing with the LYM assay using a population of 200 apparently healthy individuals in the US. This population was $56.0\%$ male, $44.0\%$ female with a mean age of 35 years. Fifty percent $(50\%)$ of the samples were collected in a non-endemic area of the US and $50\%$ in an endemic area. VIDAS LYM test values ranged from 0.00 to 0.72 with overall negativity of $87.0\%$ .
LYM Values - Analytical Specificity
| Population | N | Age (Mean) | % Male | % Female | Index Range | % Positive Results * |
| --- | --- | --- | --- | --- | --- | --- |
| Endemic | 100 | 30 | 55.0 | 45.0 | [0.00-0.72] | 12.0 |
| Vida | 100 | 30 | 55.0 | 45.0 | [0.00-0.72] | 12.0 |
| Vida + VIDAS | 100 | 30 | 55.0 | 45.0 | [0.00-0.72] | 12.0 |
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| Non-Endemic | 100 | 41 | 57.0 | 43.0 | [0.00-0.61] | 14.0 |
| --- | --- | --- | --- | --- | --- | --- |
| All samples | 200 | 35 | 56.0 | 44.0 | [0.00-0.72] | 13.0 |
* includes positive and equivocal results.
Method Comparison Study: The table below shows the results of a prospective study conducted in an endemic area of the US. This study included samples from 975 patients subjected to routine Lyme disease testing. The population was 44.9% male, 55.1% female with a mean age of 44 years. VIDAS LYM test values ranged from 0.00 to 6.14 with overall positivity of 13.9%.
LYM Values – Method Comparison
| Population | N | Age (Mean) | % Male | % Female | Index Range | % Positive Results |
| --- | --- | --- | --- | --- | --- | --- |
| Site 1 | 200 | 45 | 48.5 | 51.5 | [0.00-5.52] | 6.5 |
| Site 2 | 434 | 44 | 43.3 | 56.7 | [0.00-6.14] | 14.5 |
| Site 3 | 341 | 44 | 44.9 | 55.1 | [0.00-5.48] | 17.6 |
| All samples | 975 | 44 | 44.9 | 55.1 | [0.00-6.14] | 13.9 |
## N. Proposed Labeling:
The labeling is sufficient and it satisfies the requirements of 21 CFR Part 809.10.
## O. Conclusion:
The submitted information in this premarket notification is complete and supports a substantial equivalence decision.
