(37 days)
Not Found
No
The device description and intended use are purely mechanical, and there is no mention of AI/ML terms, image processing for analysis, or performance studies related to algorithmic output.
No.
The device is a cement restrictor used in orthopedic surgeries, not for treating or diagnosing a disease or condition.
No
The device is described as a "cement restrictor" used in orthopedic surgeries like hip and knee replacements to prevent cement migration. Its function is to physically restrict cement, not to diagnose a condition.
No
The device description clearly states it is a physical, implantable device made of PEEK with gold wire markers, not software.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections.
- Device Function: The Scient'x Cement Restrictor is a physical implant used during orthopedic surgery to restrict the flow of bone cement. It is a surgical tool/implant, not a diagnostic test performed on a sample.
- Intended Use: The intended use clearly states it's for use in orthopedic surgeries involving the femoral canal and tibial plateau. This is a surgical procedure, not a diagnostic process.
The information provided about the device's description, materials, and use in surgery confirms it is a medical device used in vivo (within the body) during a surgical procedure, not an in vitro diagnostic test.
N/A
Intended Use / Indications for Use
The Scient'x Cement Restrictor is intended as a cement restrictor in orthopedic surgeries such as those involving the femoral canal and tibial plateau in hip stem and total knee replacement.
This device is not intended for any spinal indications. The safety and effectiveness of this device when implanted in the spine have not been established.
Product codes
JDK
Device Description
The Scient'x Cement Restrictor is a hollow trapezoidal block with 1mm toothed serrations on opposite sides to prevent migration and has a threaded hole on the superior surface to attach an insertion tool. The parts are machined from PEEK that conforms to ASTM F2026-02. As peek is radiolucent gold wire radiographic markers inserted into small holes and serve as location and orientation markers for radiographs.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
femoral canal, tibial plateau
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)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 878.3300 Surgical mesh.
(a)
Identification. Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.(b)
Classification. Class II.
0
:
Scient'x Cement Restrictor 510(k) Summary
| Date | August 26, 2005 | OCT 5 - 2005 |
|---|---|---|
| Submitter | Scient'x | |
| Batiment Calypso Parc Ariane 3 | ||
| 78284 Guyancourt | ||
| FRANCE | ||
| Contact person | J.D. Webb | |
| 1001 Oakwood Blvd | ||
| Round Rock, TX 78681 | ||
| 512-388-0199 | ||
| Trade Name | Scient'x Cement Restrictor | |
| Common name | Cement restrictor | |
| Classification name | Class II per 21 CFR section 888.3300 | |
| Product Code | JDK | |
| Equivalent Device | RABEAT™ Cement Restrictor (Signus Medical, K020836) | |
| Fortitude™ Cement Restrictor (Spinal Concepts, K031837) | ||
| Device Description | The Scient'x Cement Restrictor is a hollow trapezoidal block with 1mm | |
| toothed serrations on opposite sides to prevent migration and has a | ||
| threaded hole on the superior surface to attach an insertion tool. The parts | ||
| are machined from PEEK that conforms to ASTM F2026-02. As peek is | ||
| radiolucent gold wire radiographic markers inserted into small holes and | ||
| serve as location and orientation markers for radiographs. | ||
| Intended Use | The Scient'x Cement Restrictor is intended as a cement restrictor in | |
| orthopedic surgeries such as those involving the femoral canal and tibial | ||
| plateau in hip stem and total knee replacement. |
This device is not intended for any spinal indications. The safety and
effectiveness of this device when implanted in the spine have not been
established. | |
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 entwined around it. The caduceus is a common symbol associated with healthcare and medicine. The text "DEPARTMENT OF HEALTH AND HUMAN SERVICES - USA" is arranged in a circular pattern around the caduceus symbol.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 5 - 2005
Scient'x c/o Mr. J.I). Webb Authorized Contact Person The OrthoMedix Group, Inc. 1001 Oakwood Boulevard Round Rock, Texas 78681
Re: K052367
Trade/Device Name: Scient'x Cement Restrictor Regulation Number: 21 CFR 878.3300 Regulation Name: Surgical mesh Regulatory Class: II Product Code: JDK Dated: August 26, 2005 Received: September 1, 2005
Dear Mr. Webb:
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). You may, therefore, market the device, subject to the general controls provisions of the Act and the limitations described below. 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.
The Office of Device Evaluation has determined that there is a reasonable likelihood that this device will be used for an intended use not identified in the proposed labeling and that such use could cause harm. Therefore, in accordance with Section 513(i)(1)(E) of the Act, the following limitation must appear in the Warnings section of the device's package insert and also as a Warning on the product label:
THIS DEVICE IS NOT INTENDED FOR ANY SPINAL WARNING: INDICATIONS.
THE SAFETY AND EFFECTIVENESS OF THIS DEVICE WHEN IMPLANTED IN THE SPINE HAVE NOT BEEN ESTABLISHED.
2
Please note that the above labeling limitations are required by Section 513(i)(1)(E) of the Act. Therefore, a new 510(k) is required before these limitations are modified in anv way or removed from the device's labeling.
The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and permits your device to proceed to the market. This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification if the limitation statement described above is added to your labeling.
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 bc 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.
If you desire specific information about the application of other labeling requirements to your device (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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-frec number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Donna-Bea Tillman, Ph.D., M.P.A. Director Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
Indications for Use
510(k) Number (if known): KOSZ367
Device Name: Scient'x Cement Restrictor
Indications for Use:
The Scient'x Cement Restrictor is intended as a cement restrictor in orthopedic surgeries such as those involving the femoral canal and tibial plateau in hip stem and total knee replacement.
This device is not intended for any spinal indications. The safety and effectiveness of this device when implanted in the spine have not been established.
Prescription Use X Over-The-Counter Use AND/OR (Part 21 CFR 801 Subpart D) (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
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Concurrence of CDRH, Office of Device Evaluation (ODE)
Mark H. Milliken
(Division Sign-Off) Division of General, Restorative, and Neurological Devices
510(k) Number
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A