(24 days)
No
The summary describes a mechanical hip implant and does not mention any software, algorithms, or data processing that would indicate the use of AI/ML. The "Mentions AI, DNN, or ML" and "Mentions image processing" sections are explicitly marked as "Not Found".
Yes
The device is a hip prosthesis, which is an implant used to replace a damaged hip joint, directly treating severe hip pain and disability due to various conditions.
No
The device description clearly states it is a "single use only implant that is used to replace a hip joint," which is a therapeutic function, not a diagnostic one. The intended use also lists conditions for which the hip is replaced, further indicating a treatment rather than diagnosis.
No
The device description clearly states it is a "single use only implant" and a "wedge-shaped prosthesis," indicating it is a physical medical device, 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 Description and Intended Use: The provided information clearly describes a surgical implant used to replace a hip joint. It is a physical device inserted into the body during surgery.
- Lack of IVD Characteristics: There is no mention of analyzing biological samples, detecting biomarkers, or providing diagnostic information based on laboratory testing.
This device falls under the category of a surgical implant or prosthesis, not an IVD.
N/A
Intended Use / Indications for Use
Total hip replacement for the following: severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, avascular necrosis of the femoral head, nonunion of previous fractures of the femur; congenital hip dysplasia, protrusio acetabuli, slipped capital femoral epiphysis; disability due to previous fusion; previously failed endoprostheses, and/or total hip components in the affected extremity and acute femoral neck fractures.
Hemi-hip replacement for the following: fracture dislocation of the hip; elderly, debilitated patients when a total hip replacement is contraindicated; irreducible fractures in which adequate fixation cannot be obtained; certain high subcapital fractures and comminuted femoral neck fractures in the aged; nonunion of femoral neck fractures; secondary avascular necrosis of the femoral head; pathological fractures of the femoral neck; and osteoarthritis in which the femoral head is primarily affected.
Product codes
LPH
Device Description
The Trabecular Metal Primary Hip Prosthesis is intended to be a single use only implant that is used to replace a hip joint.
The wedge-shaped prosthesis is designed for cementless use and is circumferentially bonded with Trabecular Metal over the proximal body region for biological fixation. The hip is offered in a broad range of sizes designed to accommodate varying patient anatomy with standard and extended neck offsets.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Hip joint
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)
Non-clinical testing demonstrated that the Trabecular Metal Primary Hip Prosthesis is as safe and effective as its predicate device. Clinical data and conclusions were not needed for this device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
VerSys™ Hip System - Fiber Metal Taper Hip Prosthesis, manufactured by Zimmer, Inc., K964769
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 888.3358 Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis.
(a)
Identification. A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip 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 has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.(b)
Classification. Class II.
0
Image /page/0/Picture/0 description: The image contains the word "zimmer" in bold, black font. To the left of the word is a circle with a bold, black letter "Z" inside. The letter "Z" is stylized with sharp angles and thick lines. The overall design appears to be a logo or brand mark.
Summary of Safety and Effectiveness
JUN 3 0 2005
| Submitter: | Zimmer, Inc.
P.O. Box 708
Warsaw, IN 46581-0708 |
|---------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Contact Person: | Dalene T. Binkley, RAC
Senior Associate, Regulatory Affairs
Telephone: (574) 372-4907
Fax: (574) 372-4605 |
| Date: | June 24, 2005 |
| Trade Name: | Trabecular Metal™ Primary Hip Prosthesis |
| Common Name: | Total Hip Prosthesis |
| Classification Name
and Reference: | LPH
21 CFR § 888.3358 |
| Predicate Device: | VerSys™ Hip System - Fiber Metal Taper Hip
Prosthesis, manufactured by Zimmer, Inc.,
K964769, cleared February 13, 1997 |
| Device Description: | The Trabecular Metal Primary Hip Prosthesis is
intended to be a single use only implant that is used
to replace a hip joint.
The wedge-shaped prosthesis is designed for
cementless use and is circumferentially bonded with
Trabecular Metal over the proximal body region for
biological fixation. The hip is offered in a broad
range of sizes designed to accommodate varying
patient anatomy with standard and extended neck
offsets. |
| Intended Use: | Total hip replacement for the following: severe hip
pain and disability due to rheumatoid arthritis,
osteoarthritis, traumatic arthritis, polyarthritis,
collagen disorders, avascular necrosis of the
femoral head, nonunion of previous fractures of the
femur; congenital hip dysplasia, protrusio acetabuli,
slipped capital femoral epiphysis; disability due to |
1
previous fusion; previously failed endoprostheses, and/or total hip components in the affected extremity and acute femoral neck fractures.
Hemi-hip replacement for the following: fracture dislocation of the hip; elderly, debilitated patients when a total hip replacement is contraindicated; irreducible fractures in which adequate fixation cannot be obtained; certain high subcapital fractures and comminuted femoral neck fractures in the aged; nonunion of femoral neck fractures; secondary avascular necrosis of the femoral head; pathological fractures of the femoral neck; and osteoarthritis in which the femoral head is primarily affected.
The Trabecular Metal Primary Hip Prosthesis is packaged, manufactured, and sterilized using the same materials and processes as the predicate device. The subject device also has the same intended use and fixation methods as the predicate device.
Comparison to Predicate Device:
Performance Data (Nonclinical and/or Clinical):
Non-Clinical Performance and Conclusions:
Non-clinical testing demonstrated that the Trabecular Metal Primary Hip Prosthesis is as safe and effective as its predicate device.
Clinical Performance and Conclusions:
Clinical data and conclusions were not needed for this device.
2
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States. The seal features a stylized eagle with three stripes on its wing, representing the three branches of government. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle.
Public Health Service
JUN 3 0 2005
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Ms. Dalene T. Binkley, RAC Senior Associate, Regulatory Affairs Zimmer Incorporated P. O. Box 708 Warsaw, Indiana 46581-0708
Re: K051491
K031491
Trade/Device Name: Trabecular Metal™ Primary Hip Prosthesis Regulation Number: 21 CFR 888.3358 Regulation Name: Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis Regulatory Class: II Product Code: LPH Dated: June 03, 2005 Received: June 06, 2005
Dear Ms. Binkley:
We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your becamed the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the encrosary to regary to regars and the Medical Device Amendments, or to conninered pror to May 20, 1977)
devices that have been reclassified in accordance with the provisions of the Federal Food, DNA de vices that have been require approval of a premarket approval application (PMA). alla Cosmetic Free (110) that so device, subject to the general controls provisions of the Act. The r ou may, mercere, mance and act include requirements for annual registration, listing of gencial controld provisioning 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 If your device is exassined controls. Existing major regulations affecting your device can may or subject to back access 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 I least of advisou that I Dris brisean that your device complies with other requirements of the Act that I Dri has made a aond regulations administered by other Federal agencies. You must or any I ederal bithe 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 CFR Part 807), adomig (21 CFR Part 820); and if applicable, the electronic 101th m and quants of oversions (Sections 531-542 of the Act); 21 CFR 1000-1050.
3
Page 2 - Ms. Dalene T. Binkley, RAC
This letter will allow you to begin marketing your device as described in your Section 510(k) I his letter will anow you to begin hankeling your averal equivalence of your device to a legally premarket nothcation. The PDA midning of substance vice and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Patt 801), please If you desire specific advice for your act (240) 276-0120. Also, please note the regulation entitled, p conlier the Office of Complance at (110) = i = = = = = = = = "Misbranding by relective to premarker noulities under the Act from the Division of Small other general Information on your response in to toll-free number (800) 638-2041 or and index html Manufacturers, Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours.
Sincerely, yours,
Miriam C. Provost, Ph.D.
riam C. Provost, Ph.D. Acting Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
Indications for Use
510(k) Number (if known): KOSTY9 |
Device Name:
Trabecular Metal™ Primary Hip Prosthesis
Indications for Use:
Total hip replacement for the following: severe hip pain and disability due to rheumatoid I otal hip replacement for the forlowing: 6078.0 the read as orders, avascular necrosis
arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, arthrills, osteballinitis, traintatio artifical poryal and the femur; congenital hip dysplasia, of the lemoral nead, nonumon of provious navisis; disability due to previous fusion;
protrusio acetabuli, slipped capital femoral epiphysis; disability of a flusted astronic protrusio acetabuli, shpped capital temoral opplify only somponents in the affected extremity and acute femoral neck fractures.
Hemi-hip replacement for the following: fracture dislocation of the hip; elderly, debiliated Hemi-hip replacement is contraindicated; irreducible fractures in which patients when a total inp replacement is contralized, or in the subcapital fractures and comminuted adequate fractures in the aged; nonunion of femoral neck fractures; secondary avasculars and femoral neck fractures in the aged, nonanon of formoral neck, and osteoarthritis in which the femoral head is primarily affected.
Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
(Please do not write below this line - Continue on another page if needed)
Concurrence of CDRH, Office of Device Evaluation (ODE)
| (Division Sign-Off) | |
|---|---|
| Division of General, Restorative, and Neurological Devices | |
| 510(k) Number | K051491 |
| Page 1 of 1 |
0009