(211 days)
Not Found
No
The 510(k) summary describes a mechanical interference screw for surgical fixation and contains no mention of AI, ML, image processing, or data-driven performance metrics.
No.
The device is an interference screw used for fixation of grafts during ligament reconstruction, which is a structural component rather than a device intended to treat or cure a disease or condition in a therapeutic manner.
No
Explanation: The device description states its intended use is for fixation of grafts during ligament reconstruction, which is a therapeutic intervention, not a diagnostic one.
No
The device description clearly identifies it as a physical interference screw, which is a hardware component used in surgical procedures.
Based on the provided information, the Mitek Biocryl Rapide Interference Screw is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for the fixation of soft tissue or bone tendon bone grafts during cruciate ligament reconstruction surgeries of the knee. This is a surgical procedure performed in vivo (within the living body).
- Device Description: The description is of a physical implantable device (a screw).
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (like blood, urine, tissue) in vitro (outside the body) to provide information about a physiological state, health, or disease.
IVD devices are used to perform tests on samples taken from the body, not to be implanted within the body for structural support or fixation.
N/A
Intended Use / Indications for Use
The Biocryl Rapide Interference Screw is intended for fixation of soft tissue or bone tendon bone grafts during cruciate ligament reconstruction surgeries of the knee.
Product codes (comma separated list FDA assigned to the subject device)
HWC
Device Description
The Mitek Biocryl Rapide Interference Screw
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
knee
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)
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
§ 888.3040 Smooth or threaded metallic bone fixation fastener.
(a)
Identification. A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.(b)
Classification. Class II.
0
MAR 3 1 2004
K032717 pg. '14
510(k) Summary of Substantial Equivalence
Pursuant to §513(i)(3)(A) of the Food, Drug, and Cosmetic Act, Mitek Worldwide is required to submit with this Premarket Notification either an "…adequate summary of any information respecting safety and effectiveness or state that such information will be made available upon request of any person." Mitek Worldwide chooses to submit a summary of information respecting safety and effectiveness. According to §513(i)(3)(B), "Any summary under subparagraph (A) respecting a device shall contain detailed information regarding data concerning adverse health effects ... "
1. MANUFACTURER:
Mitek Worldwide A division of Ethicon A Johnson & Johnson Company 249 Vanderbilt Avenue Norwood, MA 02062
Contract: Karen K. Sylvia, RA Manager Date Prepared: 28 August 2003
2. DEVICE:
| Trade name: | Biocryl Rapide Interference Screw |
|---|---|
| Classification Name: | Screw, Fixation Bone |
| Product Code: | HWC |
| Classification: | 888.3040 |
| Common Name: | Orthopedic Screw, Fixation Device |
3. PREDICATE DEVICE:
The predicate device used to determine substantial equivalence for the Mitek's Biocryl Rapide Interference Screws is the Biocryl Interference Screws (K013572) currently marketed by Mitek Worldwide, Norwood, MA 02062.
4. DEVICE DESCRIPTION:
The Mitek Biocryl Rapide Interference Screw
5. INTENDED USE:
The Biocryl Rapide Interference Screw is intended for fixation of soft tissue or bone tendon bone grafts during cruciate ligament reconstruction surgeries of the knee.
6. Safety and Performance:
1
K03-717
pge 2 of
The determination of substantial equivalence for this device was based on a detailed device description, conformance to consensus standards and voluntary standards.
Based on the indications for use, technological characteristics, and comparison to the predicate device, the Mitek Biocryl Rapide Interference Screw has been shown to be substantially equivalent to the predicate device under the Federal Food, Drug and Cosmetic Act.
2
Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of an eagle with three lines representing its wings.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAR 3 1 2004
Ms. Karen K. Sylvia Regulatory Affairs Manager Mitek Worldwide A Division of Ethicon A Johnson & Johnson Company 249 Vanderbilt Avenue Norwood, MA 02062
Re: K032717
Trade/Device Name: Biocryl Rapide Interference Screw Regulation Number: 21 CFR 888.3040 Regulation Name: Smooth or threaded metallic bone fixation fastener Regulatory Class: II Product Code: HWC Dated: January 8, 2004 Received: January 12, 2004
Dear Ms. Sylvia:
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.
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.
3
Page 2 - Ms. Karen K. Sylvia
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 (301) 594-4659. 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 may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
for Mark N. Wilkerson
Celia M. Witten, Ph.D., M.D. Director
Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
510(k) Number (if known) Device Name
Biocryl Rapide Interference Screw
Indications for Use
The Mitek Biocryl Rapide Interference Screw is indicated for fixation of soft tissue grafts or bone-tendon-bone grafts during cruciate ligament reconstruction surgeries of the knee.
(Please do not write below this line - Continue on another page if necessary) Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use Y A (Per 21 CFR § 801. 09)
OR
Over-the-Counter Use No
(Optional Format 1-2-96)
for Mark N Milker
(Division Sign-Off)
Division of General, Restorative, and Neurological Devices
510(k) Number K032717