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510(k) Data Aggregation

    K Number
    K222701
    Device Name
    MANTA Laser
    Manufacturer
    Date Cleared
    2022-11-18

    (72 days)

    Product Code
    Regulation Number
    878.4810
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    MANTA Laser

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The MANTA810 diode laser is indicated for use in surgical applications requiring the vaporization, incision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Cyneology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.

    The MANTA980 diode laser is indicated for use in surgical application, incision, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.

    The MANTA1064 diode laser is indicated for use in surgical applications requiring the vaporization, incision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics. Podiatry, Arthroscopy, Spinal Surgery, Gyneology, Pulmonary Surgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.

    The MANTA1470 diode laser is indicated for use in surgical applications requiring the vaporization, incision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.

    The MANTA1940 diode laser is indicated for use in surgical applications requiring the vaporization, incision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gyneology, Pulmonary Surgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.

    Device Description

    The MANTA diode lasers are a family of products with a laser diode as the beam source. Dependent on the chosen diode, the laser system can radiate one factory set wavelength with any of the following: 810nm, 980nm, 1064nm, 1470nm or 1940nm.

    The MANTA is a compact diode laser with a high-resolution color touchscreen for user control.

    AI/ML Overview

    The provided document is a 510(k) premarket notification for the MANTA Laser Family. It focuses on establishing substantial equivalence to a predicate device (Quanta Diode Laser Family, K100558) rather than presenting a study to prove acceptance criteria for device performance in the way clinical diagnostic AI/ML products typically do.

    Therefore, much of the requested information regarding a study proving acceptance criteria for AI performance (e.g., sample size for test sets, data provenance, expert qualifications, ground truth establishment, MRMC studies, standalone performance, training set details) is not applicable or available in this document.

    The document primarily addresses the safety and performance of a laser surgical instrument, which is a hardware device, through adherence to recognized international standards and comparison of technical specifications.

    Here's an analysis based on the available information:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document does not explicitly state "acceptance criteria" in the context of a performance study for AI. Instead, it compares the technical specifications of the MANTA device to a predicate device to demonstrate substantial equivalence. The "performance testing" section refers to adherence to safety and electrical standards.

    SpecificationPredicate Device (Quanta) Performance (K100558)Subject Device (MANTA) Reported PerformanceSubstantial Equivalence
    Regulation Number21 CFR 878.481021 CFR 878.4810Equivalent
    Product CodeGEXGEXEquivalent
    Regulatory ClassClass IIClass IIEquivalent
    Laser mediaDiode laserDiode laserEquivalent
    Use of deviceRX onlyRX onlyEquivalent
    Max. power (Watts)30 – 808nm, 30 – 980nm, 30 – 1064nm, 15 – 1470nm, 5 - 1950nm28 – 810nm, 28 – 980nm, 24 – 1064nm, 12 – 1470nm, 5 – 1940nmEquivalent
    Wavelength (nm)808, 980, 1064, 1470, 1950810, 980, 1064, 1470, 1940Equivalent
    Laser class44Equivalent
    Output ModeCW, pulsed, single pulseCW, pulsed, single pulseEquivalent
    Pulse Duration3 msec – 2.5 sec adjustable10 msec – 30 sec adjustableEquivalent
    Pulse frequency0.016 - 250 Hz0.02 – 50 HzEquivalent
    Aiming BeamRed 650nm (
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