(59 days)
No
The device description and performance testing focus on mechanical delivery of bone graft material and do not mention any AI/ML components or functions.
No.
Explanation: The device is intended for the delivery of bone graft material, not for directly treating a disease or condition. Its function is to facilitate a surgical procedure by delivering material, rather than providing therapy itself.
No
This device is for delivering autograft or allograft bone graft material to an orthopaedic surgical site, not for diagnosis.
No
The device description clearly lists multiple physical components (Graft Cartridge, Bone Scoop Accessory, Pack Tool Accessory, Delivery Cannula, Delivery Plunger) which are hardware.
Based on the provided information, the Avitus® DragonWing Large Volume Autograft Delivery System is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Intended Use: The intended use is to deliver bone graft material to an orthopaedic surgical site. This is a surgical procedure performed directly on the patient's body.
- Device Description: The device is a mechanical system for handling and delivering bone graft. It does not involve testing or analyzing samples taken from the body (like blood, urine, tissue, etc.) to diagnose a condition.
- Lack of IVD Characteristics: There is no mention of the device being used for diagnostic purposes, analyzing biological samples, or providing information about a patient's health status based on in vitro testing.
IVD devices are specifically designed to be used in vitro (outside the body) for the examination of specimens derived from the human body to provide information for diagnostic, monitoring, or compatibility purposes. The Avitus® DragonWing system operates in vivo (within the body) during a surgical procedure.
N/A
Intended Use / Indications for Use
The Avitus® DragonWing Large Volume Autograft Delivery System is intended to be used for the delivery of autograft or hydrated allograft bone graft material to an orthopaedic surgical site.
Product codes (comma separated list FDA assigned to the subject device)
FMF
Device Description
The Avitus® Dragonwing™ Large Volume Autograft Delivery System is designed to deliver bone autograft or hydrated allograft material to an orthopaedic surgical site. The device delivers approximately up to 5cc of bone graft material per each reloadable five-channel cartridge. Each system comes with the following:
- · 2 x Graft Cartridge Features 5 graft channels, a latching lid, and connection points to the Delivery Cannula.
- · 1 x Bone Scoop Accessory Used to add graft to the Graft Cartridge channels.
- · 1 x Pack Tool Accessory Used to compress graft into the Graft Cartridge channels.
- · 1 x Delivery Cannula Features a handle frame which connects to a loaded Graft Cartridge and a straight-tipped cannula through which graft material is delivered to the orthopaedic surgical site.
- · 1 x Delivery Plunger Features a plunger rod and handle. During graft delivery, the Delivery Plunger is pushed through a Graft Cartridge channel to deploy graft material to the orthopaedic surgical site.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
orthopaedic surgical site.
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 (study type, sample size, AUC, MRMC, standalone performance, key results)
Device performance testing included worst-case non-clinical testing in which the Avitus® Dragonwing™ Large Volume Autograft Delivery System was used to deliver cadaveric bone graft material. Testing found that the Avitus® Dragonwing™ Large Volume Autograft Delivery System meets the reliability and confidence requirements for successful delivery and for structural integrity during normal use.
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.
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
§ 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
July 17, 2023
Image /page/0/Picture/1 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: a symbol on the left and the text "FDA U.S. FOOD & DRUG ADMINISTRATION" on the right. The symbol on the left is the Department of Health & Human Services logo. The text is in blue, with "FDA" in a larger font size than the rest of the text.
Avitus Orthopaedics, Inc. % Robert Mclain Sr. Quality and Regulatory Affairs Consultant Keystone Regulatory Services, LLC 324 E. Main Street, Suite 207 Leola, Pennsylvania 17540
Re: K231456
Trade/Device Name: Avitus® DragonWing Large Volume Autograft Delivery System Regulation Number: 21 CFR 880.5860 Regulation Name: Piston Syringe Regulatory Class: Class II Product Code: FMF Dated: May 18, 2023 Received: May 19, 2023
Dear Mr. Mclain:
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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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
1
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 of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Jesse Muir -S
Jesse Muir, Ph.D. Assistant Director DHT6C: Division of Restorative, Repair and Trauma Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
Form Approved: OMB No. 0910-0120 Expiration Date: 06/30/2023 See PRA Statement below.
| 510(k) Number ( if known ) | K231456 |
|---|---|
| ----------------------------------- | --------- |
Device Name
Avitus® DragonWing Large Volume Autograft Delivery System
Indications for Use (Describe)
The Avitus® DragonWing Large Volume Autograft Delivery System is intended to be used for the delivery of autograft or hydrated allograft bone graft material to an orthopaedic surgical site.
| Type of Use (Select one or both, as applicable) | Prescription Use (Part 21 CFR 801 Subpart D) Over-The-Counter Use (21 CFR 801 Subpart C) |
|---|---|
| ------------------------------------------------- | ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- |
CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the
time to review instructions, search existing data sources, gather and maintain the data needed and complete
and review the collection of information. Send comments regarding this burden estimate or any other aspect
of this information collection, including suggestions for reducing this burden, to:
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"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB number."
FORM FDA 3881 (6/20)
|| ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
3
Section 1
510(k) Summary
Submission Owner and Correspondent 1.1
Submission Owner
Avitus Orthopaedics, Inc. 6 Armstrong Rd., 2nd Floor Shelton, CT 06484 USA Contact: Maxim Budyansky Phone: 860-372-7213 Email: maxim@avitusortho.com
Submission Correspondent
Keystone Regulatory Services, LLC 342 E. Main Street, Suite 207 Leola, PA 17540 Contact: Robert McLain Phone: 717-656-9656 E-Mail: rob.mclain@keystoneregulatory.com
Date Summary Prepared 1.2
July 17, 2023
1.3 Device Trade Name
Avitus® Dragonwing™ Large Volume Autograft Delivery System
Device Common Name 1.4
Piston syringe.
1.5 Device Classification Name
Syringe, Piston Classified as Class 2 at 21 CFR 880.5860, product code FMF.
4
Legally Marketed Device To Which The Device Is Substantially 1.6 Equivalent
The Avitus® Dragonwing TM Large Volume Autograft Delivery System is substantially equivalent to the Spinal Surgical Strategies, LLC Bi-Portal Bone Graft Delivery Device cleared under K142661.
Description of the Device 1.7
The Avitus® Dragonwing™ Large Volume Autograft Delivery System is designed to deliver bone autograft or hydrated allograft material to an orthopaedic surgical site. The device delivers approximately up to 5cc of bone graft material per each reloadable five-channel cartridge. Each system comes with the following:
- · 2 x Graft Cartridge Features 5 graft channels, a latching lid, and connection points to the Delivery Cannula.
- · 1 x Bone Scoop Accessory Used to add graft to the Graft Cartridge channels.
- · 1 x Pack Tool Accessory Used to compress graft into the Graft Cartridge channels.
- · 1 x Delivery Cannula Features a handle frame which connects to a loaded Graft Cartridge and a straight-tipped cannula through which graft material is delivered to the orthopaedic surgical site.
- · 1 x Delivery Plunger Features a plunger rod and handle. During graft delivery, the Delivery Plunger is pushed through a Graft Cartridge channel to deploy graft material to the orthopaedic surgical site.
Indications for Use 1.8
The Avitus® Dragonwing™ Large Volume Autograft Delivery System is intended to be used for the delivery of autograft or hydrated allograft bone graft material to an orthopaedic surgical site.
1.9 Technological Characteristics
Table 1.1 compares the technological characteristics of the proposed Avitus® Dragonwing TM Large Volume Autograft Delivery System and the predicate Bi-Portal Bone Graft Delivery Device.
This section contains a comparison of technological characteristics of the Avitus® Dragonwing™ Large Volume Autograft Delivery System and the predicate Bi-Portal Bone Graft Delivery Device and, where there are differences, provides an explanation of why there is no negative impact on substantial equivalence.
5
| Feature | Proposed Device - Avitus® DragonwingTM
Large Volume Autograft Delivery System | Predicate Device -
Bi-Portal Bone
Graft Delivery
Device (K142661) |
|------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------|
| Product Code | FMF; Syringe, Piston | FMF; Syringe, Piston |
| Classification
and Regulation | Class 2; 880.5860 | Class 2; 880.5860 |
| Indication for
Use | Intended to be used for the delivery of bone
autograft or hydrated allograft. | Intended to be used for
the delivery of bone
autograft or hydrated
allograft. |
| Materials | Biocompatible Polycarbonate (Graft Cartridge,
Cannula, Plunger, and Bone Scoop and Pack Tool
Accessories)
Biocompatible Stainless Steel (Cannula and
Plunger) | Biocompatible Plastics
(Entire Device) |
| Mechanism of
Operation | Graft material dispersed from device tip by
depressing the plunger. | Graft material
dispersed from device
tip by depressing the
plunger. |
| Recommended
Graft Volume | Approximately up to 5.0cc per Cartridge | Up to 4.0cc in Barrel |
| Bone Graft Exit
Hole
Configuration | Single cannula endhole; 4.6mm diameter | Two sideholes; 5.6mm x
14.8mm |
| Sterilization
Method | Ethylene Oxide | Ethylene Oxide |
Table 1.1: Device Comparison
Materials
Both the Avitus® Dragonwing™ Large Volume Autograft Delivery System and the predicate K142661 Bi-Portal Bone Graft Delivery Device are made of biocompatible plastic materials. All elements of Avitus Dragonwing M Large Volume Autograft Delivery System are composed of polycarbonate with the sole exception of the cannula and plunger components, which contain biocompatible stainless steel in addition to polycarbonate. The polycarbonate and stainless steel materials which make up the Avitus® Dragonwing™ Large Volume Autograft Delivery System are identical to the polycarbonate and stainless steel materials which make up the Avitus Orthopaedics, Inc. Bone Harvester devices (K152474). Similarities in Avitus® Dragonwing TM Large Volume Autograft Delivery System and Avitus Bone Harvester device scale, manufacturing methods, and intended clinical use environment indicate that materials will not negatively impact the overall use and function of the new device. Biocompatibility has been demonstrated with the utilization of identical materials and processes to the materials found in the currently-cleared Avitus Orthopaedics, Inc. Bone Harvester devices, there is no negative impact on product safety or effectiveness.
6
Recommended Graft Volume
The predicate K142661 Bi-Portal Bone Graft Delivery Device can accommodate up to 4.0 cc of hydrated allograft or autograft material in its syringe barrel. The Avitus® Dragonwing TM Large Volume Autograft Delivery System can accommodate approximately up to 5.0 cc of hydrated allograft or autograft material in each 5-channel reloadable Graft Cartridge (approximately up to 1.0 cc of graft material per channel). Each Cartridge channel can accommodate approximately up to 1.0 cc of material. If more graft is required at the delivery site, the user replaces the Graft Cartridge with another loaded Graft Cartridge. This is repeated as many times as needed by opening the lid of the spent Graft Cartridge and reloading it after bone delivery. The Avitus® Dragonwing™ Large Volume Autograft Delivery System and the predicate K142661 Bi-Portal Bone Graft Delivery Device are intended to deliver slightly different volumes of graft. There is no negative impact of recommended graft volume on product safety or effectiveness because the Avitus® Dragonwing™ Large Volume Autograft Delivery System will be utilized by clinicians who want to deliver a large quantity of graft materials in small increments.
Bone Graft Exit Hole Configuration
The predicate K142661 Bi-Portal Bone Graft Delivery Device deploys bone autograft or hydrated allograft through bilateral sideholes. Each sidehole measures 14.8 mm x 5.6 mm. The Avitus® Dragonwing TM Large Volume Autograft Delivery System deploys bone autograft or hydrated allograft through a single endhole in the distal tip of the Delivery Cannula. The Cannula has an exit hole diameter of 4.6 mm. This difference indicates that the devices are designed to deliver graft material at different rates based on user preference, however, there is no difference between the proposed and predicate devices in terms of function and intended purpose. The Avitus® Dragonwing TM Large Volume Autograft Delivery System effectively delivers graft material. This has been demonstrated in performance testing. There is no negative impact of the difference in bone graft exit hole configuration on product safety or effectiveness.
Non-Clinical Testing 1.10
Avitus Orthopaedics, Inc. performed device performance testing, sterilization validation, package integrity testing, shelf-life testing, and biocompatibility testing (cytotoxicity, sensitization, irritation/intracutaneous reactivity, acute systemic toxicity, and material-mediated pyrogenicity).
Device performance testing included worst-case non-clinical testing in which the Avitus® Dragonwing™ Large Volume Autograft Delivery System was used to deliver cadaveric bone graft material. Testing found that the Avitus® Dragonwing™ Large Volume Autograft Delivery System meets the reliability and confidence requirements for successful delivery and for structural integrity during normal use.
1.11 Biocompatibility
The materials which make up the Avitus® Dragonwing™ Large Volume Autograft Delivery System are identical to the materials which make up the Avitus Orthopaedics, Inc. Bone Harvester devices (K152474). These materials were found to be biocompatible as part of that submission.
Clinical Testing 1.12
No clinical testing was performed in association with this submission.
7
1.13 Conclusions
The results of the comparison of design, materials, intended use, and technological characteristics The results of the companson of deagh, mondou ass, monitive of themselves cannons and effective as the legally marketed predicate devices.