(91 days)
Not Found
No
The document describes a mechanical lipoplasty system and a reagent for tissue digestion. There is no mention of AI or ML in the intended use, device description, or performance studies.
No.
The device is intended for the fragmentation, emulsification, and aspiration of soft tissue and subcutaneous fatty tissues for aesthetic body contouring or waste digestion, which are not therapeutic uses.
No
Explanation: The provided text describes the device as being used for fragmentation, emulsification, and aspiration of soft tissues for surgical procedures and aesthetic body contouring. It does not mention any function related to diagnosing medical conditions.
No
The device description clearly outlines physical components: a Lipoplasty Unit (a single-use disposable device with a cannula and collection canister) and a Celase Reagent (a single-use reagent). This indicates a hardware-based medical device, not a software-only one.
Based on the provided text, the Cytori Lipoplasty System with Celase Reagent is not an IVD (In Vitro Diagnostic) device.
Here's why:
- Intended Use: The intended use is for surgical procedures involving the fragmentation, emulsification, and aspiration of soft tissue and subcutaneous fatty tissues within the patient's body for purposes like aesthetic body contouring and tissue removal. This is a surgical device used directly on the patient.
- Device Description: The device description confirms it's a system for removing tissue from the patient and processing it within a collection canister for waste disposal.
- Lack of Diagnostic Purpose: The device's function is entirely focused on tissue removal and processing for surgical or waste management purposes. There is no mention of analyzing the tissue or bodily fluids to provide diagnostic information about a patient's health condition.
- Celase Reagent Function: The Celase Reagent is used to digest waste tissue after it has been removed from the patient, primarily to prevent clogging in the waste system. This is a processing step for waste, not a diagnostic test.
IVD devices are specifically designed to perform tests on specimens (like blood, urine, tissue samples) taken from the human body to provide information for the diagnosis, monitoring, or treatment of a disease or condition. The Cytori Lipoplasty System does not fit this description.
N/A
Intended Use / Indications for Use
The Cytori Lipoplasty System is intended for use in the following surgical specialties when the fragmentation, emulsification, and aspiration of soft tissue is desired:
- Neurosurgery
- Gastrointestinal and Affiliated Organ Surgery
- Urological Surgery
- Plastic and Reconstructive Surgery
- General Surgery
- Orthopedic Surgery
- Gynecological Surgery
- Thoracic Surgery
- Laparoscopic Surgery
The Cytori Lipoplasty System is indicated for use when the fragmentation, emulsification, and aspiration of subcutaneous fatty tissues for aesthetic body contouring is desired.
The Celase Reagent is intended for use in the fragmentation, emulsification, disaggregation, and liquefaction of soft tissues and subcutaneous fatty tissues within the Lipoplasty System's collection canister.
Product codes (comma separated list FDA assigned to the subject device)
MUU, QPB
Device Description
The Cytori Lipoplasty System with Celase Reagent is provided in two packaged assemblies: 1). Lipoplasty The Cyton Lipoplasty of the Lipoplasy Unit is a single-use disposable device designed to utilize house Offit 2). Colast Reagent: The Elipopulasy Only of Carrers. vacuum to create suction within the hollow liposuction cannula and remove subcutaneous fatty tissue from the patient and transport the adipose tissue into the collection canister. The Celase Reagent is a single-use, non-reusable reagent designed to digest the waste tissue in the collection canister as a means to allow the non-reasons rought designed the screen and mitigate down-stream clogging and blockage in the waste system.
The Cytori Lipoplasty System is a sterile, single-use, manual device consisting of a cannula, connection tric cyton Lipopulate collection container that relies on house vacuum for its energy supply. The preassembled Lipoaspirate Unit alleviates assembly errors at the point of care and prevents the misuse of incompatible parts. The cannula handle is attached to the collection canister via connection tubing. The moonline parts. Into cain a single opening near the tip to communicate house vacuum to the tissues and subsequently fragment, emulsify, and aspirate subcutaneous fatty tissues from the patient into the waste collection canister for purposes of aesthetic body contouring. The tip is fabricated from medical waste beinener canable is parposes bricated from medical grade polypropylene. The connection tubing grade stamled from medical grade polyvinyl chloride (PVC) that is DEHP free. The waste collection container is fabricated from medical grade polycarbonate to assure robustness in the operating room environment. The collection canister contains various capped/sealed reagent ports and a 1190 micron filter to trap large tissue masses while allowing liquified tissue to pass through to a hospital-provided collection trap. This mechanism prevents large tissue masses from accumulating and subsequently clogging downstream tubing that could interfere with vacuum.
The Lipoplasty cannula is provided in various sizes ranging from 15cm - 36cm in length and 3.0 - 4.6mm in diameter with a single opening near the tip of the cannula. The tip region of the cannula may have a single or multiple openings that range in size from 4mm to 12mm in length distributed uniformly or randomly throughout the end of the cannula. The handle of the device is 20mm in diameter and may be rancomily in diameters ranging from 20mm in diameter. The connecting tubing is provided with provided in acter of 9.6mm (3/8"), an outer diameter of 14.3mm (9/16"), and a wall thickness of 2.2mm. The tubing that connects the cannula handle to the waste canister is provided in a length of 4 feet and may be provided in lengths ranging from 1 - 8 feet. The bottom of the waste collection container is also provided with the same 3/8" inner diameter connection tubing of various lengths. The proximal end of the exiting connection tubing may be provided with a barbed tubing connector to assist in the attachment of like-sized tubing for purposes of connecting the Cytori Lipoplasty System to house vacuum and/or assorted waste traps. Connection tubing leading to and from the waste collection container is provided with a stepped clamp to facilitate manual control of the vacuum supplied to the cannula. The stepped clamps also allow the operator to seal the connection tubing on both sides of the collection canister and prevent spillage of the collected fluids/tissues, thereby facilitating safe transport and disposal of the waste materials.
The Celase Reagent is a mixture of proteolytic enzymes provided in 70mg lyophilized powder form packaged in a single-use unit consisting of an amber vial with a rubber stopper and associated screw-top cap within a foam-protected aluminum canister.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Soft tissue, subcutaneous fatty tissues
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Surgical specialties (Neurosurgery, Gastrointestinal and Affiliated Organ Surgery, Urological Surgery, Plastic and Reconstructive Surgery, General Surgery, Orthopedic Surgery, Gynecological Surgery, Thoracic Surgery, Laparoscopic Surgery)
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)
Mechanical testing of the Cytori Lipoplasty System with Celase Reagent demonstrates that the device is substantially equivalent to the predicate.
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.
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
§ 878.5040 Suction lipoplasty system.
(a)
Identification. A suction lipoplasty system is a device intended for aesthetic body contouring. The device consists of a powered suction pump (containing a microbial filter on the exhaust and a microbial in-line filter in the connecting tubing between the collection bottle and the safety trap), collection bottle, cannula, and connecting tube. The microbial filters, tubing, collection bottle, and cannula must be capable of being changed between patients. The powered suction pump has a motor with a minimum of1/3 horsepower, a variable vacuum range from 0 to 29.9 inches of mercury, vacuum control valves to regulate the vacuum with accompanying vacuum gauges, a single or double rotary vane (with or without oil), a single or double diaphragm, a single or double piston, and a safety trap.(b)
Classification. Class II (special controls). Consensus standards and labeling restrictions.
0
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
Cytori Therapeutics, Inc. Kenneth Kleinhenz Sr. Director, RA 3020 Callan Road San Diego, California 92121-1109
June 8, 2021
Re: K063235
Trade/Device Name: Cytori Lipoplasty System With Celase Reagent Regulation Number: 21 CFR 878.5040 Regulation Name: Suction lipoplasty system Regulatory Class: Class II Product Code: QPB
Dear Kenneth Kleinhenz:
The Food and Drug Administration (FDA) is sending this letter to notify you of an administrative change related to your previous substantial equivalence (SE) determination letter dated January 24, 2007. Specifically, FDA is updating this SE Letter because FDA has created a new product code to better categorize your device technology.
Please note that the 510(k) submission was not re-reviewed. For questions regarding this letter please contact Cindy Chowdhury, OHT4: Office of Surgical and Infection Control Devices, 240-402-6647, Cindy.Chowdhury@fda.hhs.gov.
Sincerely,
Cindy Chowdhury -S
Cindy Chowdhury, Ph.D., M.B.A. Assistant Director DHT4B: Division of Infection Control and Plastic Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
1
Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized caduceus symbol, which is a staff with two snakes coiled around it. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the caduceus symbol. The logo is black and white.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Cytori Therapeutics, Inc. % Mr. Kenneth K. Kleinhenz Sr. Director of Regulatory Affairs 3020 Callan Road San Diego, California 92121
JAN 2 4 2007
Re: K063235
Trade/Device Name: Cytori Lipoplasty System with Celase Reagent Regulation Number: 21 CFR 878.5040 Regulation Name: Suction lipoplasty system Regulatory Class: II Product Code: MUU Dated: January 5, 2007 Received: January 9, 2007
Dear Mr. Kleinhenz:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce ass blated in 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) that do not require approval of a premarket approval application (PMA). 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 (PMA), 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 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
2
Page 2 -- Mr. Kenneth K. Kleinhenz
This letter will allow you to begin marketing your device as described in your Section 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), please contact the Office of Compliance at (240) 276-0115. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Mark N. Molkerson
Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
8063235 Indications for Use
Device Name: Cytori Lipoplasty System with Celase Reagent
Indications for Use:
The Cytori Lipoplasty System is intended for use in the following surgical specialties when the fragmentation, emulsification, and aspiration of soft tissue is desired:
- · Neurosurgery
- · Gastrointestinal and Affiliated Organ Surgery
- · Urological Surgery
- · Plastic and Reconstructive Surgery
- · General Surgery
- · Orthopedic Surgery
- · Gynecological Surgery
- · Thoracic Surgery
- · Laparoscopic Surgery
The Cytori Lipoplasty System is indicated for use when the fragmentation, emulsification, and aspiration of subcutaneous fatty tissues for aesthetic body contouring is desired.
The Celase Reagent is intended for use in the fragmentation, emulsification, disaggregation, and liquefaction of soft tissues and subcutaneous fatty tissues within the Lipoplasty System's collection canister.
Prescription Use X (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
| Concurrence of CDRH, Office of Device Evaluation (ODE) | |
|---|---|
| CITY |
(Division Sign-Off)
Division of General, Restorative,
and Neurological Devices
510(k) Number 63236
Page 1 of 1
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ADMINISTRATIVE INFORMATION
| Manufacturer Name: | Cytori Therapeutics, Inc.
3020 Callan Road
San Diego, CA 92121
JAN 24 2001 |
|--------------------|--------------------------------------------------------------------------------------------------------------|
| Official Contact: | Kenneth K. Kleinhenz
Sr. Director of Regulatory Affairs
Telephone (858) 458-0900
Fax (858) 458-0994 |
DEVICE NAME
Classification Name: Trade/Proprietary Name: Suction Lipoplasty System Cytori Lipoplasty System with Celase Reagent
EST ABLISHMENT REGISTRATION NUMBER 2031733
DEVICE CLASSIFICATION AND PRODUCT CODE
As shown in 21 CFR 878.5040, Suction Lipoplasty Systems are defined as devices consisting of collection bottles, cannulas, and connecting tubing for use in aesthetic body contouring procedures. Suction Lipoplasty Systems are classified as Class II. They have been assigned Product Code MUU.
INTENDED USE
The Cytori Lipoplasty System is intended for use in the following surgical specialties when the fragmentation, emulsification, and aspiration of soft tissue is desired:
- · Neurosurgery
- · Gastrointestinal and Affiliated Organ Surgery
- · Urological Surgery
- · Plastic and Reconstructive Surgery
- · General Surgery
- · Orthopedic Surgery
- · Gynecological Surgery
- · Thoracic Surgery
- · Laparoscopic Surgery
The Cytori Lipoplasty System is indicated for use when the fragmentation, and aspiration of subcutaneous fatty tissues for aesthetic body contouring is desired.
The Celase Reagent is intended for use in the fragmentation, disaggregation, and liquefaction of soft tissues and subcutaneous fatty tissues within the Lipoplasty System's Collection Canister.
5
DEVICE DESCRIPTION
Design Characteristics
Design Characteristics
The Cytori Lipoplasty System with Celase Reagent is provided in two packaged assemblies: 1). Lipoplasty The Cyton Lipoplasty of the Lipoplasy Unit is a single-use disposable device designed to utilize house Offit 2). Colast Reagent: The Elipopulasy Only of Carrers.
vacuum to create suction within the hollow liposuction cannula and remove subcutaneous fatty tissue from the patient and transport the adipose tissue into the collection canister. The Celase Reagent is a single-use, non-reusable reagent designed to digest the waste tissue in the collection canister as a means to allow the non-reasons rought designed the screen and mitigate down-stream clogging and blockage in the waste system.
Lipoplasty Unit
The Cytori Lipoplasty System is a sterile, single-use, manual device consisting of a cannula, connection tric cyton Lipopulate collection container that relies on house vacuum for its energy supply. The preassembled Lipoaspirate Unit alleviates assembly errors at the point of care and prevents the misuse of incompatible parts. The cannula handle is attached to the collection canister via connection tubing. The moonline parts. Into cain a single opening near the tip to communicate house vacuum to the tissues and subsequently fragment, emulsify, and aspirate subcutaneous fatty tissues from the patient into the waste collection canister for purposes of aesthetic body contouring. The tip is fabricated from medical waste beinener canable is parposes bricated from medical grade polypropylene. The connection tubing grade stamled from medical grade polyvinyl chloride (PVC) that is DEHP free. The waste collection container is fabricated from medical grade polycarbonate to assure robustness in the operating room environment. The collection canister contains various capped/sealed reagent ports and a 1190 micron filter to trap large tissue masses while allowing liquified tissue to pass through to a hospital-provided collection trap. This mechanism prevents large tissue masses from accumulating and subsequently clogging downstream tubing that could interfere with vacuum.
The Lipoplasty cannula is provided in various sizes ranging from 15cm - 36cm in length and 3.0 - 4.6mm in diameter with a single opening near the tip of the cannula. The tip region of the cannula may have a single or multiple openings that range in size from 4mm to 12mm in length distributed uniformly or randomly throughout the end of the cannula. The handle of the device is 20mm in diameter and may be rancomily in diameters ranging from 20mm in diameter. The connecting tubing is provided with provided in acter of 9.6mm (3/8"), an outer diameter of 14.3mm (9/16"), and a wall thickness of 2.2mm. The tubing that connects the cannula handle to the waste canister is provided in a length of 4 feet and may be provided in lengths ranging from 1 - 8 feet. The bottom of the waste collection container is also provided with the same 3/8" inner diameter connection tubing of various lengths. The proximal end of the exiting connection tubing may be provided with a barbed tubing connector to assist in the attachment of like-sized tubing for purposes of connecting the Cytori Lipoplasty System to house vacuum and/or assorted waste traps. Connection tubing leading to and from the waste collection container is provided with a stepped clamp to facilitate manual control of the vacuum supplied to the cannula. The stepped clamps also allow the operator to seal the connection tubing on both sides of the collection canister and prevent spillage of the collected fluids/tissues, thereby facilitating safe transport and disposal of the waste materials.
Celase Reagent
The Celase Reagent is a mixture of proteolytic enzymes provided in 70mg lyophilized powder form packaged in a single-use unit consisting of an amber vial with a rubber stopper and associated screw-top cap within a foam-protected aluminum canister.
6
Material Composition
Material Composition
The components of the Cytori Lipoplasty System that have patient contact are fabricated from surgical stainless steel. The Celase Reagent is a lyophilized blend of buffered salts and proteolytic enzymes
Sterility
Stermy aseptically and sterile filtered.
In Vitro Testing
Mechanical testing of the Cytori Lipoplasty System with Celase Reagent demonstrates that the device is substantially equivalent to the predicate.
EQUIVALENCE TO MARKETED PRODUCT
The Cytori Lipoplasty System with Celase Reagent shares indications and design principles with the following predicate device which has been determined by FDA to be substantially equivalent to a preamendment device: MacroPore Lipoplasty System (K042261), Flow Laboratories Trypsin (K771955) and Oxoid USA Sputasol (K802493); Class II medical devices that were cleared for marketing in the United States under K042261, K771955, and K802493 respectively.
Indications For Use
The Cytori Lipoplasty System with Celase Reagent and the MacroPore Lipoplasty System predicate device share substantially equivalent indications for use as they are both indicated for the fragmentation, emulsification and aspiration of soft tissues in aesthetic body contouring procedures and are indicated for the same surgical specialties. The Cytori Lipoplasty System with Celase Reagent shares indications for use language with the predicate devices.
Design and Materials
The design and materials of Cytori Lipoplasty System with Celase Reagent and the predicate device (MacroPore Lipoplasty System) are substantially equivalent as they both utilize a hollow tubular cannulas attached to a handle. The cannula tip of the subject device and the predicate devices contains one or several openings to allow communication between the applied vacuum and the patient's tissues. The Cytori Lipoplasty System with Celase Reagent and the MacroPore Purice! Lipoplasty System predicate device are substantially equivalent in design as they both consist of a cannula, connection tubing, and a waste collection container. The waste collection containers on the Cytori Lipoplasty System with Celase Reagent and the MacroPore Puricel Lipoplasty System predicate device are provided in substantially equivalent volume capacities. The Cytori Lipoplasty System with Celase Reagent and the predicate devices (Trypsin and Sputasol Reagents) are substantially equivalent as they all enzymatically digest tissues and cells in vitro.