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510(k) Data Aggregation

    K Number
    K181007
    Device Name
    Cianna Medical SAVI Scout Reflector and SAVI Scout System
    Manufacturer
    Cianna Medical, Inc.
    Date Cleared
    2018-08-02

    (107 days)

    Product Code
    NEU
    Regulation Number
    878.4300
    Why did this record match?
    Applicant Name (Manufacturer) :

    Cianna Medical, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Scout Reflector is intended to be placed percutaneously in soft tissue to mark (>30 days) a biopsy site or a soft tissue site intended for surgical removal. Using imaging guidance (such as ultrasound, MRI, or radiography) or aided by non-imaging guidance (SAVI Scout System) the SAVI Scout Reflector is located and surgically removed with the target tissue. The SAVI Scout System is intended only for the non-imaging detection and localization of the SAVI Scout Reflector that has been implanted in a soft tissue biopsy site or a soft tissue site intended for surgical removal.
    Device Description
    Not Found
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    K Number
    K171767
    Device Name
    Cianna Medical SAVI Scout Reflector and SAVI Scout System
    Manufacturer
    Cianna Medical, Inc.
    Date Cleared
    2017-10-31

    (139 days)

    Product Code
    NEU
    Regulation Number
    878.4300
    Why did this record match?
    Applicant Name (Manufacturer) :

    Cianna Medical, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Scout Reflector is intended to be placed percutaneously in breast tissue to mark (>30 days) a biopsy site or a lumpectomy site intended for surgical removal. Using imaging guidance (such as ultrasound, MRI, or radiography) or aided by non-imaging guidance (SAVI Scout System) the SAVI Scout Reflector is located and surgically removed with the target tissue. The SAVI Scout System is intended only for the non-imaging detection and localization of the SAVI Scout Reflector that has been implanted in a breast biopsy site or a lumpectomy site intended for surgical removal.
    Device Description
    Not Found
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    K Number
    K161507
    Device Name
    Cianna Medical SAVI Scout Reflector and SAVI Scout System
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2016-07-29

    (58 days)

    Product Code
    PDW, PBY
    Regulation Number
    878.4670
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Scout Reflector is intended to be placed percutaneously in the breast to temporarily mark (<30days) a lumpectomy site intended for surgical removal. Using imaging guidance (such as ultrasound or radiography) or aided by non-imaging guidance (SAVI Scout System) the SAVI Scout Reflector is located and surgically removed with the target tissue. The SAVI Scout System is intended only for the non-imaging detection and localization of the SAVI Scout Reflector that has been implanted in a lumpectomy site intended for surgical removal.
    Device Description
    SAVI Scout Reflector and SAVI Scout System
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    K Number
    K141318
    Device Name
    CIANNA MEDICAL SGS SYSTEM
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2014-08-27

    (99 days)

    Product Code
    PDW, PBY
    Regulation Number
    878.4670
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Cianna Medical SGS Tissue Marker is intended to be placed percutaneously in the breast to temporarily (< 7 days) mark a lumpectomy site intended for surgical removal. Using imaging guidance (such as ultrasound or radiography) or aided by non-imaging guidance (SGS System) the SGS Tissue Marker is located and surgically removed with the target tissue. The SGS System is intended only for the non-imaging detection of the "SGS Marker" that has been implanted in a lumpectomy site intended for surgical removal.
    Device Description
    Not Found
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    K Number
    K132463
    Device Name
    CIANNA MEDICAL PERMANENT TISSUE MARKER AND DELIVERY SYSTEM
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2013-12-03

    (118 days)

    Product Code
    NEU
    Regulation Number
    878.4300
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Cianna Medical Permanent Tissue Marker is intended to mark tissue during a percutaneous breast biopsy procedure and be permanently visible by radiography and visible for up to thirty days by ultrasound.
    Device Description
    The Cianna Medical Permanent Tissue Marker and Delivery System consists of an implantable marker and a delivery system. The marker is comprised of a series of 1 mm diameter titanium "beads" which are constrained onto a heat shaped nitinol wire. The marker is preloaded within the lumen of the delivery system. Once percutaneously deployed from the delivery system, the marker maintains a coiled shape (approximately 4.5mm diameter by 5mm length) within the tissue. The marker is echogenic under Ultrasound, radiopaque under radiograph imaging. The Cianna Medical Permanent Tissue Marker and Delivery System is provided sterile, and is for single use only.
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    K Number
    K101411
    Device Name
    SAVI PREPARATION DEVICE
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2010-07-12

    (54 days)

    Product Code
    JAQ, JAO
    Regulation Number
    892.5700
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Preparation Device is temporarily implanted in the lumpectomy to access the lumpectomy cavity, aid in the selection of the appropriate SAVI brachytherapy applicator and serve as a placeholder until it is exchanged for the SAVI brachytherapy applicator.
    Device Description
    The SAVI Preparation Device is a specialized catheter with an inflatable balloon at the distal end. The SAVI Preparation Device is temporarily implanted in the lumpeon at the access the lumpectomy cavity, aid in the selection of the appropriate SAVI brachytheray applicator and serve as a placeholder until it is exchanged for the SAVI brachytherapy applicator. The SAVI Preparation Device is provided sterile for single use and is disposable.
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    K Number
    K081677
    Device Name
    SAVI APPLICATOR KIT
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2008-07-22

    (35 days)

    Product Code
    JAQ
    Regulation Number
    892.5700
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Applicator is intended for use as an accessory to commercially available remote afterloading equipment used during brachytherapy procedures. The multiple lumens of the SAVI Applicator are intended to provide pathways from which a prescribed radiation dose is delivered to the treatment area.
    Device Description
    The SAVI Applicator is an expandable cylindrical device with radially positioned catheters, which is inserted into the target volume. The SAVI Applicator is provided sterile and is a single use device.
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    K Number
    K080565
    Device Name
    MODIFICATION TO: SAVI APPLICATOR KIT
    Manufacturer
    CIANNA MEDICAL, INC.
    Date Cleared
    2008-04-04

    (35 days)

    Product Code
    JAQ
    Regulation Number
    892.5700
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIANNA MEDICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SAVI Applicator Kit is intended for use as an accessory to commercially available remote afterloading equipment used during brachytherapy procedures. The multiple lumens of the SAVI Applicator are intended to provide pathways from which a prescribed radiation dose is delivered to the treatment area.
    Device Description
    The SAVI Applicator is an expandable cylindrical device with radially positioned catheters, which is inserted into the target volume. The SAVI Applicator is provided sterile and is a single use device.
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