(123 days)
Not Found
No
The summary describes a mechanical implant and an external controller, with no mention of AI/ML terms or functionalities.
Yes
Explanation: The device is indicated for fracture fixation, pseudoarthrosis, or mal-unions and non-unions of long bones, which are medical conditions that require treatment. Its function is to correct or alleviate these conditions.
No
The device is an orthopedic implant (nail system) used for fracture fixation and repair in long bones. It is a treatment device, not a diagnostic one.
No
The device description clearly outlines hardware components including a nail, locking screws, surgical instruments, and an external remote controller (ERC). It also mentions the nail contains a magnet, lead screw/nut assembly, and planetary gearing. This is not a software-only device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for "open and closed fracture fixation, pseudoarthrosis, or mal-unions and non-unions of long bones." This describes a surgical implant used to treat bone conditions.
- Device Description: The description details a mechanical implant (nail, screws, instruments, external controller) designed to be inserted into the body to stabilize bones.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (like blood, urine, or tissue) outside of the body to provide information about a person's health. IVDs are typically used for diagnosis, monitoring, or screening based on in vitro analysis.
The device described is a surgical implant used for orthopedic procedures, which falls under a different regulatory category than IVDs.
N/A
Intended Use / Indications for Use
The Ellipse PRECICE Trauma Nail System is 15270indicated for open and closed fracture fixation, pseudoarthrosis, or mal-unions and nonunions of long bones.
Product codes (comma separated list FDA assigned to the subject device)
HSB
Device Description
The PRECICE Trauma Nail System is composed of the PRECICE Trauma Nail (supplied sterile), locking screws, surgical instruments and an external remote controller (ERC or ERC 2P). The Nail is available in various diameters, lengths and screw-hole configurations to accommodate a variety of patient anatomies. The locking screws are also available in a variety of diameters and lengths. The PRECICE Trauma Nail is supplied sterile by gamma radiation while the locking screws and instruments are supplied non-sterilized prior to use. The Nail contains an enclosed rare earth magnet, telescoping lead screw/nut assembly, and planetary gearing. The Nail is supplied pre-distracted by 10 mm (femur and tibia models), 15 mm and 20 mm (humeral model) to allow for compression fracture reduction techniques.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
long bones, humerus
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
Non-clinical testing of the PRECICE Trauma Nail System included design verification testing to ensure the device meets the retraction (compression) force and distraction force required for the humerus and cadaveric design validation testing to ensure the device can be inserted into the medullary canal and fixed to the humerus using the humeral specific instruments. The following specific performance tests were completed on the PRECICE Trauma Nail System in order to establish equivalence to the predicate device:
Test Description: Device Functionality and Verification
Applicable Test Standard: N/A
Test Description: Design Validation
Applicable Test Standard: N/A
Non-clinical testing that was submitted for the predicate PRECICE Trauma Nail System which are applicable to the subject device include mechanical testing according to the methods outlined in the standard ASTM F1264-03, validation of the gamma radiation sterilization cycle in accordance with the VDmas methodology as given in ISO 11137-2 to verify that the gamma radiation sterilization process provides a sterility assurance level of 10-, shelf life testing for the packaging after accelerated aging, Oring seal performance testing and biocompatibility in accordance with ISO 10993-1 for the intended use of the device.
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
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
§ 888.3020 Intramedullary fixation rod.
(a)
Identification. An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.(b)
Classification. Class II.
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 seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized design featuring a symbol that resembles a human figure or a caduceus, composed of three curved lines.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
December 22, 2015
Ellipse Technologies Incorporated John McIntyre Vice President, Regulatory, Clinical, Quality Affairs 13900 Alton Parkway Suite 123 Irvine, California 92618
Re: K152370
Trade/Device Name: PRECICE Trauma Nail System Regulation Number: 21 CFR 888.3020 Regulation Name: Intramedullary Fixation Rod Regulatory Class: Class II Product Code: HSB Dated: August 20, 2015 Received: August 21, 2015
Dear John McIntyre:
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 devicerelated 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.
1
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/ResourcesforYou/Industry/default.htm. 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
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,
Casey Hanley -S
Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
510(k) Number (if known)
Device Name
PRECICE® Trauma Nail System
Indications for Use (Describe)
The Ellipse PRECICE Trauma Nail System is 15270indicated for open and closed fracture fixation, pseudoarthrosis, or mal-unions and nonunions of long bones.
Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)
| Over-The-Counter Use (21 CFR 801 Subpart C)
PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.
FOR FDA USE ONLY
Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)
3
Image /page/3/Picture/1 description: The image shows the logo for Ellipse. The logo consists of three overlapping circles on the left, with the word "ELLIPSE" in blue to the right of the circles. The circles are colored in shades of blue and green. The word "ELLIPSE" is in a sans-serif font.
101 Enterprise, Suite 100 Aliso Viejo, CA 92656-2604 Office: 949-837-3600 949-837-3664 Fax" www.ellispe-tech.com
PRECICE Trauma Nail System 510(k) Summary August 2015
-
- Company: Ellipse Technologies, Incorporated 101 Enterprise Suite 100 Aliso Viejo, CA 92656
- Contact: John McIntyre VP, Regulatory, Clinical and Quality Affairs Phone: (949) 837-3600 x203 Fax: (949) 837-3664
Date of Submission: August 19, 2015
-
- Proprietary Trade Name: PRECICE Trauma Nail System
- Classification Name: Intramedullary Fixation Rod (21 CFR 888.3020) 3.
-
- Product Code: HSB (Rod, Fixation, Intramedullary and Accessories)
- Product Description: The PRECICE Trauma Nail System is composed of the PRECICE Trauma Nail (supplied sterile), locking screws, surgical instruments and an external remote controller (ERC or ERC 2P). The Nail is available in various diameters, lengths and screw-hole configurations to accommodate a variety of patient anatomies. The locking screws are also available in a variety of diameters and lengths. The PRECICE Trauma Nail is supplied sterile by gamma radiation while the locking screws and instruments are supplied non-sterilized prior to use. The Nail contains an enclosed rare earth magnet, telescoping lead screw/nut assembly, and planetary gearing. The Nail is supplied pre-distracted by 10 mm (femur and tibia models), 15 mm and 20 mm (humeral model) to allow for compression fracture reduction techniques.
Indications: The Ellipse PRECICE Trauma Nail System is indicated for open and closed fracture 6. fixation, pseudoarthrosis, or mal-unions and non-unions of long bones.
- Substantial equivalence: A detailed comparison to the predicate device demonstrates that the Ellipse PRECICE Trauma Nail System is substantially equivalent to the following 510(k) cleared device:
| Trade Name: | PRECICE® Trauma Nail System |
|---|---|
| Common Name: | Intramedullary Fixation Rod |
| 510(k) Clearance Number: | K142599 |
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K152370 - Page 2 of 2
Image /page/4/Picture/1 description: The image shows the logo for Ellipse. On the left side of the logo are three overlapping circles in shades of blue and green. To the right of the circles is the word "ELLIPSE" in a bold, sans-serif font. The word is in a dark blue color.
101 Enterorise, Suite 100 Aliso Vieio. CA 92656-26 949-837-3600 949-837-366 www.ellispe-tech.com
Substantial equivalence is based on same indications for use, technological characteristics, principles of operation, designs, and on in vitro testing performed.
The modified PRECICE Trauma Nail System subject to this Special 510(k) and the predicate system have the same indications for use. Specifically, both systems are indicated for open and closed fracture fixation, pseudoarthrosis, or mal-unions and non-unions of long bones. This Special 510(k) is intended to include models specific for the humerus.
The modified Ellipse PRECICE Trauma Nail System has similar technological characteristics and the same principles of operation as that of the predicate. Both the current PRECICE Trauma Nails and the additional Humeral Trauma Nail models subject of this Special 510(k) are titanium intramedullary nails with a telescoping portion that can adjust the limb using principles of distraction osteogenesis. Both devices are inserted into the intramedullary canal of the long bone and secured with PRECICE locking screws. Both devices are adjusted non-invasively by the Ellipse External Remote Controller (ERC). The differences between the two devices are dimensional to better fit the anatomy and fixation requirements of the humerus, and the pre-distracted length of the device.
Non-clinical testing of the PRECICE Trauma Nail System included design verification testing to ensure the device meets the retraction (compression) force and distraction force required for the humerus and cadaveric design validation testing to ensure the device can be inserted into the medullary canal and fixed to the humerus using the humeral specific instruments. The following specific performance tests were completed on the PRECICE Trauma Nail System in order to establish equivalence to the predicate device:
| Test Description | Applicable Test Standard |
|---|---|
| Device Functionality and Verification | N/A |
| Design Validation | N/A |
Non-clinical testing that was submitted for the predicate PRECICE Trauma Nail System which are applicable to the subject device include mechanical testing according to the methods outlined in the standard ASTM F1264-03, validation of the gamma radiation sterilization cycle in accordance with the VDmas methodology as given in ISO 11137-2 to verify that the gamma radiation sterilization process provides a sterility assurance level of 10-, shelf life testing for the packaging after accelerated aging, Oring seal performance testing and biocompatibility in accordance with ISO 10993-1 for the intended use of the device.
There are no changes to the design of the ERC being made as a result of this submission, therefore all testing that was submitted for the ERC in the predicate PRECICE Trauma Nail System is applicable to the modified PRECICE Trauma Nail System.
Conclusions can be drawn from these tests that the modified Trauma Nail System with the Humeral Trauma Nail line extension is substantially equivalent to the predicate device.