(108 days)
Not Found
No
The document describes a mechanical hip implant and its intended uses, materials, and testing. There is no mention of software, algorithms, or any technology related to AI or ML.
Yes
The device is a hip replacement system intended to restore patient range of motion and treat deformities resulting from various conditions like arthritis and necrosis, which are therapeutic functions.
No
The device description indicates it is a "Fenoral Hip Stem" for surgical implantation to restore range of motion and treat deformities, not to diagnose medical conditions.
No
The device description clearly states it is a "Femoral Hip Stem," which is a physical implant made of titanium alloy or cobalt chrome. The summary also details mechanical and dynamic testing, which is typical for hardware components, not software.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use describes a surgical implant for replacing parts of the hip joint to treat conditions like arthritis, fractures, and necrosis. This is a therapeutic intervention performed in vivo (within the body).
- Device Description: The device is a physical component (femoral hip stem) made of metal alloys, designed to be surgically implanted.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening.
IVD devices are used in vitro (outside the body) to analyze biological samples. This device is a surgical implant used in vivo.
N/A
Intended Use / Indications for Use
- When used as a hemi-hip replacement system, it is intended for osteo-, rheumatoid, and post-traumatic arthritis of the hip with minimal involvement of the corresponding acetabulum, femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
- When used as a total hip replacement system, it is intended for osteo-, rheumatoid, and post-traumatic arthritis of the hip with minimal involvement of the corresponding acetabulum. femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
- In addition, the SIERRA™ hip stem is intended for cases where alternative modes of trealment appear less preferable and the associated risks of a total hip replacement are thought to be acceptable. It is intended for severely disabled joints, which could result from arthritis or late stages of avascular necrosis and revisions of unsuccessful acetabular cup arthroplasty and/or femoral procedure.
Product codes
LPH, JDI, KWY
Device Description
The SIERRA™ Femoral Hip Stem is a sterile component used to help restore patient range of motion and aid in the treatment of other deformities as listed in the Indications for Use. The SIERRA™ Femoral Hip Stem has a tapered distal stem design and is available in a variety of options including cemented, porous coated or porous coated with hydroxylapatite (HA) coating. They are also available with standard or high offset necks, as well as collared and non-collared designs. This submission seeks clearance for the SIERRA™ Femoral Hip Stem, which is a line extension to the NexFlex™ Total Hip System. The SIERRA™ Femoral Hip Stem is manufactured from titanium alloy (Ti 6Al-4V, ASTM F136) or cobalt chrome (CoCrMo, ASTM F75). Cobalt chrome stems are intended for cemented use. The porous coated and HA/porous coated stems are intended for uncemented use.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Hip
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
Mechanical and dynamic testing of the SIERRA™ Femoral Hip Stem was performed.
Key Metrics
Not Found
Predicate Device(s)
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
DEC - € 2004
SIERRA™ Femoral Hip Stem 510(k) SUMMARY August 2004
- l . Company: Nexmed, Inc. 6110 Corte Del Cedro Carlsbad, CA 92009, USA (760) 431-9286
II Contact Person: Ellen Yarnall, Director of Regulatory Affairs
111 Trade/Proprietary Name: SIERRA™ Femoral Hip Stem
IV Product Description:
The SIERRA™ Femoral Hip Stem is a sterile component used to help restore patient range of motion and aid in the treatment of other deformities as listed in the Indications for Use. The SIERRA™ Femoral Hip Stem has a tapered distal stem design and is available in a variety of options including cemented, porous coated or porous coated with hydroxylapatite (HA) coating. They are also available with standard or high offset necks, as well as collared and non-collared designs. This submission seeks clearance for the SIERRA™ Femoral Hip Stem, which is a line extension to the NexFlex™ Total Hip System. The SIERRA™ Femoral Hip Stem is manufactured from titanium alloy (Ti 6Al-4V, ASTM F136) or cobalt chrome (CoCrMo, ASTM F75). Cobalt chrome stems are intended for cemented use. The porous coated and HA/porous coated stems are intended for uncemented use.
V. Classification
| LPH (21 CFR 888.3358) | Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis |
|---|---|
| JDI (21 CFR 888.3350) | Hip joint metal/polymer semi-constrained cemented prosthesis |
| KWY (21 CFR 888.3390) | Hip joint femoral (hemi-hip) metal/polymer cemented or uncemented or uncemented prosthesis. |
VI Indications for Use
-
- When used as a hemi-hip replacement system, it is intended for osteo-, rheumatoid, and post-traumatic arthritis of the hip with minimal involvement of the corresponding acetabulum, femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
-
- When used as a total hip replacement system, it is intended for osteo-, theumatoid, and posttraumatic arthritis of the hip with minimal involvement of the corresponding acetabulum. femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
-
- In addition, the SIERRA™ hip stem is intended for cases where alternative modes of trealment appear less preferable and the associated risks of a total hip replacement are thought to be acceptable. It is intended for severely disabled joints, which could result from arthritis or late stages of avascular necrosis and revisions of unsuccessful acetabular cup arthroplasty and/or femoral procedure.
1
SIERRA™ Femoral Hip Stem 510(k) SUMMARY August 2004
VII Substantial Equivalence:
The SIERRA™ Femoral Hip Stem is substantially equivalent to femoral hip stems from the following predicate devices:
Trade/Proprietary Name NexFlex™ Total Hip System Synergy HA Coated Porous Femoral Stems Synergy Cemented Hip Stems
Manufacturer Nexmed, Inc. Smith & Nephew, Inc.
Smith & Nephew, Inc.
Kago369
VIII Performance Data:
Mechanical and dynamic testing of the SIERRA™ Femoral Hip Stem was performed.
2
Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is an abstract image of an eagle with three lines representing its wings.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
DEC - 6 2004
Ms. Ellen A. Yarnall Director of Regulatory Affairs Nexmed, Inc. 6110 Corte Del Cedro Carlsbad, California 92009
Re: K042252
Tro 12/Device Name: Nexflex Total Hip System, Sierra Femoral Hip Stem Regulation Number: 21 CFR 888.3358; 21 CFR 888.3350; 21 CFR 888.3390 Regulation Name: Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis; Hip joint metal/polymer semi-constrained cemented prosthesis; Hip joint femoral (hemi-hip) metal/polymer cemented or uncemented prosthesis
Regulatory Class: II Product Code: LPH, JDI, KWY Dated: November 15, 2004 Received: November 16, 2004
Dear Ms. Yarnall:
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 docs 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
3
Page 2 - Ms. Ellen A. Yarnall
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.
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 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,
Marlie N. Millbern
Celia 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
Indications for Use
510(k) Number (if known): K042252
Device Name: _________________________________________________________________________________________________________________________________________________________________
Indications for Use:
-
- When used as a hemi-hip replacement system, it is intended for osteo-, rheumatoid, and post-traumatic arthritis of the hip with minimal involvement of the corresponding acetabulum, femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
-
- When used as a total hip replacement system, it is intended for osteo-, rheumatoid, and post-traumatic arthritis of the hip with minimal involvement of the corresponding acetabulum, femoral head or neck fractures, aseptic necrosis of the femoral head, previous failed hip arthroplasty where there is evidence of sufficient bone quality to adequately set the implant.
-
- In addition, the NexFlex™ Total Hip System is intended for cases where alternative modes of treatment appear less preferable and the associated risks of a total hip replacement are thought to be acceptable. It is intended for severely disabled joints, which could result from arthritis or late stages of avascular necrosis and revisions of unsuccessful acetabular cup arthroplasty and/or femoral procedure.
Mule N Millause
and Neurological Devices
510(k) Number K042252
Prescription Use X (Part 21 CFR 801 Subpart D)
AND/OR
Over-The Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE- CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)