(57 days)
Not Found
No
The device description and performance studies focus on mechanical functionality and material delivery, with no mention of AI or ML.
No
The device is described as a system for delivering bone graft material to an orthopedic surgical site, and it is also designed to facilitate mixing of bone graft material. It is an instrument used in a surgical procedure, not a therapeutic device itself.
No
The device is designed for the delivery of bone graft material and facilitating mixing, not for diagnosis.
No
The device description explicitly details physical components made of stainless steel, including a cannula, trocar rod, plunger rod, handle assembly, slide hammer adapter, slide hammer, and strike cap. It also mentions a disposable kit and a reusable handle assembly, all of which are hardware.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for the "delivery of allograft, autograft, and synthetic bone graft material to an orthopedic surgical site" and facilitating the "mixing and pre-mixing of bone graft material with I.V. fluids, blood, plasma concentrate, platelet-rich plasma, bone marrow or other specified blood components". This describes a surgical tool for delivering materials into the body, not a device used to examine specimens from the body to provide diagnostic information.
- Device Description: The description details a system of instruments (cannula, trocar rod, plunger rod, handle assembly) designed for accessing bone tissue and delivering materials. This aligns with a surgical device, not an IVD.
- Lack of Diagnostic Function: There is no mention of the device being used to analyze samples, detect markers, or provide any form of diagnostic information about a patient's condition.
- Anatomical Site: The indicated anatomical site (femur, humerus with early stage necrosis) is the target for the surgical procedure, not the source of a diagnostic sample.
IVD devices are used to perform tests on specimens (like blood, urine, tissue) taken from the human body to provide information for diagnosis, monitoring, or screening. The PerFuse Percutaneous Decompression System does not fit this description.
N/A
Intended Use / Indications for Use
The PerFuse Percutaneous Decompression System is intended to be used for the delivery of allograft, autograft, and synthetic bone graft material to an orthopedic surgical site. In addition, it is designed to facilitate mixing and pre-mixing of bone graft material with I.V. fluids, blood, plasma concentrate, platelet-rich plasma, bone marrow or other specified blood components deemed necessary by the clinical use requirements.
Product codes
FMF
Device Description
The disposable instrument set is comprised of a sterile, sinqle-use disposable kit containing the stainless steel cannula, trocar rod, and plunger rod. The non-sterile stainless steel handle assembly consists of a reusable handle, slide hammer adapter, slide hammer, and strike cap. The handle assembly is organized in a stainless steel instrument case. All components are made of stainless steel. The strike cap threads onto the handle body and is designed to receive a mallet or hammer strike to drive the trocar point/cannula into bone tissue.
The handle is cannulated to allow the trocar rod to pass through the length of the handle and be contained within the strike cap. The cannula creates a 6.17mm bore diameter hole.
The cannula, trocar rod, and plunger rod all come in two lengths. The cannula is designed for use in accessing the femoral head. The smaller length is designed to access the humeral head. Each cannula has depth lines etched onto the surface to indicate the instrument depth to the operating surgeon. The cannula and plunger rod and/or syringe (syringe sold separately) are used to deliver blood components and/or bone graft material through the cannula to an orthopedic surgical site.
The gamma-sterilized components are supplied as single use disposables to ensure the cannula is free of debris and the trocar rod is sharp at the beginning of each procedure.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Femur, humerus (specifically femoral head and humeral head for access)
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
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
Non-Clinical Testing: Non-clinical laboratory testing was performed. The results indicated that the devices were functional within their intended use.
Summary Table - Performance Testing - Bench:
- Cannula Luer Taper Load Test: All 18 syringes maintained a seal throughout the duration of mechanical loading without failure.
- Cannula Luer Taper Load Test – No Axial Restraint: All 18 syringes maintained a seal throughout the duration of mechanical loading without failure.
- Instrument Integrity in a sawbones simulation: All 6 cannula fully penetrated 1.4 cm into the grade 30 sawbones block. The handle could only be removed from the cannula by releasing the Zimmer-Hudson connection, leaving the cannula in place to facilitate fluid and graft material delivery.
- Instrument Cadaver Lab Verification Study: Six core decompression procedures were successfully performed using the PerFuse instrument sets (trocar + cannula).
- Delivery of hydrated graft through PerFuse and CDO cannulas: All acceptance criteria were met. The hydrated graft material was easily expressed from the syringe through the cannula with thumb pressure, at least 80% of the original graft material was delivered, and equivalence between the PerFuse and CDO delivery methods was established.
Key Metrics
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 880.5860 Piston syringe.
(a)
Identification. A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular border with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the top half. Inside the circle is an abstract symbol that resembles a stylized human figure or a bird in flight, composed of three curved lines that form the shape of a head and body.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
August 27, 2014
Biomet Biologics LLC Mr. Lonnie Witham Scientific Affairs Project Manager - Biologics P.O. Box 587 Warsaw, Indiana 46581-0587
Re: K141762
Trade/Device Name: PerFuse Percutaneous Decompression System Regulation Number: 21 CFR 880.5860 Regulation Name: Piston, Syringe Regulatory Class: II Product Code: FMF Dated: June 30, 2014 Received: July 01, 2014
Dear Mr. Witham:
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 prior to May 28, 1976, 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you; however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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); medical device reporting (reporting of medical
1
device-related adverse events) (21 CFR 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
David Krause -S
- Binita S. Ashar, M.D., M.B.A., F.A.C.S. for Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known): K141762
Device Name: PerFuse Percutaneous Decompression System
Indications for Use:
The PerFuse Percutaneous Decompression System is intended to be used for the delivery of allograft, autograft, and synthetic bone graft material to an orthopedic surgical site. In addition, it is designed to facilitate mixing and pre-mixing of bone graft material with I.V. fluids, blood, plasma concentrate, plateletrich plasma, bone marrow or other specified blood components deemed necessary by the clinical use requirements.
Prescription Use ____________________________AND/OR Subpart D)
Over-The-Counter Use NO (Part 21 CFR 801 (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation
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Image /page/3/Picture/0 description: The image shows the logo for Biomet Biologics. The word "BIOMET" is in large, bold, sans-serif font. Below that, in a smaller font, is the word "BIOLOGICS". A green line separates the word "BIOLOGICS" from the phrase "One Surgeon, One Patient" which is in a smaller font.
K141762 - Page 1
510(k) Summary Preparation Date: May 30, 2014
Applicant/Sponsor:
Biomet Biologics, LLC P.O. Box 587 Warsaw, IN 46581-0587
Contact Person:
Lonnie Witham Scientific Affairs Proiect Manager - Biologics lonnie.witham@biomet.com Tel: 574-371-3095 Fax: 574-371-1187
Trade Name: PerFuse Percutaneous Decompression System Common Name: Graft Delivery Syringe and Decompression Instrument Classification name: Piston Syringe (21 CFR 888.5860 Product Code: FMF) Regulatory Class: II
Product Name: PerFuse Percutaneous Decompression System Physical State: The delivery cannula consists of a reusable handle assembly (handle, strike plate, slide hammer) and sterile, single-use disposable cannula, trocar rod, plunger rod (stainless steel) Technical Method: Channel is cut into bone by cannula/trocar using handle/hammer. Bone graft material is hydrated, mixed and loaded into the cannula with the piston syringe and delivered through cannula with the syringe and plunger rod.
Target Area: Femur, humerus with early stage necrosis
Legally Marketed Devices To Which Substantial Equivalence Is Claimed:
CDO™ System (K072330) consists of a curved delivery cannula, a modified syringe, a flexible plunger and an optional syringe adaptor tip. The Graft Preparation System (piston syringe) was also cleared in (K072330) and can be used to mix and deliver and to enable delivery of blood components and/or bone graft materials through the cannula. These previously cleared predicate devices have the same indications for use as the Perfuse Percutaneous Decompression System.
Device Description:
The disposable instrument set is comprised of a sterile, sinqle-use disposable kit containing the stainless steel cannula, trocar rod, and plunger rod. The non-sterile stainless steel handle assembly consists of a reusable handle, slide hammer adapter, slide hammer, and strike cap. The handle assembly is organized in a stainless steel instrument case. All components are made of stainless steel. The strike cap threads onto the handle body and is designed to receive a mallet or hammer strike to drive the trocar point/cannula into bone tissue.
The handle is cannulated to allow the trocar rod to pass through the length of the handle and be contained within the strike cap. The cannula creates a 6.17mm bore diameter hole.
The cannula, trocar rod, and plunger rod all come in two lengths. The cannula is designed for use in accessing the femoral head. The smaller length is designed to access the humeral head. Each cannula has depth lines etched onto the surface to indicate the instrument depth to the operating
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K141762 – Page 2
Image /page/4/Picture/1 description: The image shows the logo for Biomet Biologics. The logo consists of the word "BIOMET" in large, bold, sans-serif font, with the word "BIOLOGICS" in a smaller font size underneath. A thin green line is placed below the word "BIOLOGICS". The text "One Surgeon, One Patient" is placed below the green line.
surgeon. The cannula and plunger rod and/or syringe (syringe sold separately) are used to deliver blood components and/or bone graft material through the cannula to an orthopedic surgical site.
The gamma-sterilized components are supplied as single use disposables to ensure the cannula is free of debris and the trocar rod is sharp at the beginning of each procedure.
Indications for Use:
The PerFuse Percutaneous Decompression System is intended to be used for the delivery of allograft, autograft, and synthetic bone graft material to an orthopedic surgical site. In addition, it is designed to facilitate mixing and pre-mixing of bone graft material with I.V. fluids, blood, plasma concentrate, platelet-rich plasma, bone marrow or other specified blood components deemed necessary by the clinical use requirements.
Summary of Technologies: The overall design and processing methods are similar to the predicate device to which substantial equivalence is claimed. The PerFuse Percutaneous Decompression System and CDO System (K072330) have the same intended use of delivering various bone grafting materials through a metal cannula to an orthopedic surgical site. Both devices are used with the Graft Preparation System (K072330).
Non-Clinical Testing: Non-clinical laboratory testing was performed. The results indicated that the devices were functional within their intended use.
| Verification Test | Results Summary |
|---|---|
| 1. Cannula Luer Taper | |
| Load Test | All 18 syringes maintained a seal throughout the |
| duration of mechanical loading without failure | |
| 2. Cannula Luer Taper | |
| Load Test – No Axial | |
| Restraint | All 18 syringes maintained a seal throughout the |
| duration of mechanical loading without failure. | |
| 3. Instrument Integrity in | |
| a sawbones simulation | All 6 cannula fully penetrated 1.4 cm into the grade |
| 30 sawbones block. The handle could only be | |
| removed from the cannula by releasing the Zimmer- | |
| Hudson connection, leaving the cannula in place to | |
| facilitate fluid and graft material delivery. | |
| 4. Instrument Cadaver | |
| Lab Verification Study | Six core decompression procedures were successfully |
| performed using the PerFuse instrument sets (trocar |
- cannula) |
| 5. Delivery of hydrated
graft through PerFuse
and CDO cannulas | All acceptance criteria were met. The hydrated graft
material was easily expressed from the syringe
through the cannula with thumb pressure, at least
80% of the original graft material was delivered, and
equivalence between the PerFuse and CDO delivery
methods was established. |
Summary Table - Performance Testing - Bench
5
K141762 – Page 3
Image /page/5/Picture/1 description: The image shows the logo for Biomet Biologics. The word "BIOMET" is in large, bold, sans-serif font. Below that, in a smaller font, is the word "BIOLOGICS". Underneath the words is a green line, and below that is the phrase "One Surgeon, One Patient."
Summary Statement
The PerFuse Percutaneous Decompression System and the CDO System have substantially equivalent characteristics including:
- . Ability to deliver hydrated graft material through the cannula
- Utilization of a metal delivery cannula (PerFuse is stainless steel & CDO is aluminum) .
- . Utilization of syringe and/or bowl for mixing and hydrating bone graft
- Plunger to advance graft material through the delivery cannula into the orthopedic ● surqical site
- Cannula and plunger rods are single use only ●
- . Identical sterilization of disposables
- . Compatibility with the previously cleared Graft Preparation System (mixing/hydrating modified syringe)
- . Biocompatible materials conforming to ASTM standards
- . Similar Biomet packaging
Conclusion. Based on the nonclinical verification testing, results show that both the CDO System and the Perfuse Percutaneous Decompression System delivered at least 80% of the original graft material. The devices have similar designs and the same indications for use. Based on the information provided in this submission, the PerFuse Percutaneous Decompression System is substantially equivalent to the predicate CDO System.