(292 days)
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No
The document describes a traditional knee implant system and does not mention any AI or ML components, image processing, or data sets typically associated with AI/ML devices.
Yes
The Saiph® Knee System is a medical device intended to reduce or relieve pain and improve knee function in patients with specific conditions, which aligns with the definition of a therapeutic device.
No
The Saiph® Knee System is a total knee replacement device mentioned for cemented use in total knee arthroplasty surgery to replace articulating surfaces and improve knee function, not to diagnose a condition.
No
The device description clearly states that the Saiph® Knee System is comprised of physical components made from materials like cast cobalt chrome and UHMWPE, intended for surgical implantation. This indicates it is a hardware medical device, not software-only.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices intended to be used in vitro for the examination of specimens, including blood, tissue, and urine, derived from the human body, solely or principally for the purpose of providing information concerning a physiological or pathological state, or concerning a congenital abnormality or to determine the safety and compatibility with potential recipients, or to monitor therapeutic measures.
- Saiph® Knee System Function: The Saiph® Knee System is a surgical implant used to replace the articulating surfaces of the knee joint. It is a physical device implanted into the body to restore function and relieve pain.
- Lack of Specimen Examination: The provided information clearly describes the device as a knee replacement system and its intended use in surgery. There is no mention of it being used to examine any biological specimens outside of the body.
Therefore, based on the provided information, the Saiph® Knee System falls under the category of a surgical implant or prosthetic device, not an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
The Saiph® Knee System is intended for cemented only in the U.S. It is intended for single use in total knee arthroplasty surgery for the reduction or relief of pain and/or improved knee function in skeletally mature patients with the following conditions:
-
Non-inflammatory degenerative joint disease resulting from osteoarthritis, traumatic arthritis and avascular necrosis;
-
Inflammatory degenerative joint disease including rheumatoid arthritis;
-
Correction of varus, valgus, or post traumatic deformity;
-
Correction or revision of unsuccessful osteotomy or arthrodesis;
-
Revision procedures where other treatments or devices have failed; and
-
Treatment of fractures that are unmanageable using other techniques.
Product codes (comma separated list FDA assigned to the subject device)
JWH
Device Description
The Saiph® Knee System is used in total knee replacement to replace articulating surfaces of the femur, tibia and patella. The device is intended for cemented fixation only. The patella is optional depending upon surgeon preference and is cemented use only. The femoral and tibial tray components are made from cast cobalt chrome. The tibial bearing and patella components are made from ultra-high molecular weight polyethylene (UHMWPE). The femoral component is highly polished to articulate with the tibial bearing. All devices are gamma irradiated.
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
Knee joint
Indicated Patient Age Range
Skeletally mature patients
Intended User / Care Setting
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Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
SUMMARY OF NON-CLINICAL TESTS
The Saiph® Knee System has been evaluated for tibial tray fatigue strength, insert locking mechanism strength, tibiofemoral range of motion, tibiofemoral range of constraint, patellofemoral range of constraint, tibiofemoral contact stress and patellofemoral contact area and contact stress. The testing confirms that the Saiph® Knee System is capable of withstanding loads in excess of those expected in vivo and is substantially equivalent to the competitive legally marketed knee systems.
SUMMARY OF CLINICAL TESTS
Clinical usage in Europe (England and Belgium) and Australia validated that the specific surgical instruments included with this system meet user needs.
A total of 127 procedures have been registered by the National Joint Registries in the UK. Maximum follow up is 4.8 years (minimum 1.6 years). There have been no reports of revisions.
A multi-center, post-market study is ongoing in the Australia and the UK with 282 implants. The implants have been followed for average 1.9 years (range 0.6 to 5 years). There have been 3 revisions.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
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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.
K020214, K023211, K003910, K963148, K031729, K935080, K931466, K932070, K946088
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).
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§ 888.3560 Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.
(a)
Identification. A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (§ 888.3027).(b)
Classification. Class II.
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other. The profiles are black against a white background.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
November 17, 2014
MatOrtho Limited % Mr. Marcos Velez-Duran President M-Squared Associates Incorporated 815 King Street Alexandria, Virginia 22314
Re: K140222
Trade/Device Name: Saiph® Knee System Regulation Number: 21 CFR 888.3560 Regulation Name: Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis Regulatory Class: Class II Product Code: JWH Dated: October 9, 2014 Received: October 14, 2014
Dear Mr. Velez-Duran:
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
1
Page 2 - Mr. Marcos Velez-Duran
(21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) 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,
Lori A. Wiggins -S
for Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indications for Use
510(k) Number (if known) K140222
Device Name Saiph® Knee System
Indications for Use (Describe)
The Saiph® Knee System is intended for cemented only in the U.S. It is intended for single use in total knee arthroplasty surgery for the reduction or relief of paintined only in the U.S. It is intended to single use in total knear patients with the following
-
- Non-inflammatory degenerative joint disease resulting from osteoarthritis and avascular necrosis;
-
- Inflammatory degenerative joint disease including rheumatoid arthritis;
-
- Correction of varus, valgus, or post traumatic deformity;
-
- Correction or revision of unsuccessful osteotomy or arthrodesis;
-
- Revision procedures where other treatments or devices have faily and
- Treatment of fractures that are unmanageable using other techniques.
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)
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| Submitter Information | |
|---|---|
| Name | MatOrtho Limited |
| Address | 13 Mole Business Park |
| Randalls Road | |
| Leatherhead | |
| Surrey | |
| KT22 7BA | |
| United Kingdom | |
| Phone number | +44 (0)1372 224 200 |
| Fax number | +44 (0)1372 366 343 |
| Establishment Registration | |
| Number | 9035148 |
| Name of contact person | Marcos Velez-Duran |
| Date prepared | October 8, 2014 |
| Name of device | |
| Trade or proprietary name | Saiph® Knee System |
| Common or usual name | Knee Prosthesis |
| Classification name | Knee joint patellofemorotibial polymer/metal/polymer semi- |
| constrained cemented prosthesis (Class II) | |
| Classification panel | Orthopedic |
| Regulation | 21 CFR 888.3560 |
| Product Code(s) | 87JWH |
| Legally marketed device(s) | |
| to which equivalence is | |
| claimed | K020214 - Medial Rotation Knee™ (MRK) System (JWH) |
| K023211 - NexGen® Complete Knee Solution Cruciate | |
| Retaining (CR)-Flex Femoral Components (JWH) | |
| K003910 - NexGen® Complete Knee Solution Crosslinked | |
| Polyethylene Cruciate Retaining (CR) Articular | |
| Surface Components (JWH) | |
| K963148 - NexGen® Complete Knee Solution (JWH) | |
| K031729 - Triathlon® PS Knee (JWH) | |
| K935080 - Insall Burstein II | |
| K931466 - PFC Modular Total Knee System | |
| K932070 - Duracon® Constrained PS Knee | |
| Reason for 510(k) | |
| submission | New device |
| Device description | The Saiph® Knee System is used in total knee replacement to |
| replace articulating surfaces of the femur, tibia and patella. | |
| The device is intended for cemented fixation only. The patella | |
| is optional depending upon surgeon preference and is | |
| cemented use only. The femoral and tibial tray components | |
| are made from cast cobalt chrome. The tibial bearing and | |
| patella components are made from ultra-high molecular | |
| weight polyethylene (UHMWPE). The femoral component is | |
| highly polished to articulate with the tibial bearing. All | |
| devices are gamma irradiated. | |
| Intended use of the device | Cemented total joint replacement intended to replace diseased |
| or severely worn articulating surfaces of the knee joint. | |
| Indications for use | The Saiph® Knee System is intended for cemented only in the |
| U.S. It is intended for single use in total knee arthroplasty | |
| surgery for the reduction or relief of pain and/or improved knee | |
| function in skeletally mature patients with the following | |
| conditions: |
-
Non-inflammatory degenerative joint disease
resulting from osteoarthritis, traumatic arthritis and
avascular necrosis; -
Inflammatory degenerative joint disease including
rheumatoid arthritis; -
Correction of varus, valgus, or post traumatic
deformity; -
Correction or revision of unsuccessful osteotomy or
arthrodesis; -
Revision procedures where other treatments or
devices have failed; and -
Treatment of fractures that are unmanageable using
other techniques. |
K946088 - Genesis® PS Knee
510(k) Summary
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5
Summary of the technologies
The Saiph® Knee System is comprised of the multiple components including femorals, tibial trays and bearings, and patella, as well as instrumentation.
The technological characteristics are the same as the predicate devices (K020214, K023211, K003910. K963148 and K031729) in terms of design. materials, and principle of operation with the exception of the slight modifications outlined in this 510(k) submission.
The femur, tibia and patellar components utilize the identical manufacturing processes as the predicate, Medial Rotation Knee™ (MRK) System (K020214). This includes the same cemented (stippled) surface and "barb" locking mechanism used for the tibial tray and tibial bearing. Non-clinical tests were used to characterize the physical aspects of the design and to demonstrate substantial equivalence to the predicate devices. A summary of physical testing is given in the Performance Data (Non-clinical) section below. Physical testing is considered acceptable and equivalent to predicate devices. Clinical evidence of the Saiph is available in Australia and Europe and the device has been in use since 2009. A summary of Clinical Data is given below.
PERFORMANCE DATA
SUMMARY OF NON-CLINICAL TESTS
Performance Test Summarv-New Device
The Saiph® Knee System has been evaluated for tibial tray fatigue strength, insert locking mechanism strength, tibiofemoral range of motion, tibiofemoral range of constraint, patellofemoral range of constraint, tibiofemoral contact stress and patellofemoral contact area and contact stress. The testing confirms that the Saiph® Knee System is capable of withstanding loads in excess of those expected in vivo and is substantially equivalent to the competitive legally marketed knee systems.
SUMMARY OF CLINICAL TESTS
Clinical usage in Europe (England and Belgium) and Australia validated that the specific surgical instruments included with this system meet user needs.
A total of 127 procedures have been registered by the National Joint Registries in the UK. Maximum follow up is 4.8 years (minimum 1.6 years). There have been no reports of revisions.
A multi-center, post-market study is ongoing in the Australia and the UK with 282 implants. The implants have been followed for average 1.9 years (range 0.6 to 5 years). There have been 3 revisions.
6
There have been no device related failures.
CONCLUSIONS DRAWN FROM NON-CLINICAL AND CLINICAL DATA
The Saiph® Knee System was found to be substantially equivalent to the predicate devices based on non-clinical testing. Clinical data from the National Joint Registry in the UK and data from a post-market clinical study being conducted in Australia and the UK show that the Saiph® Knee System is safe and effective. There have been no device related failures.