(83 days)
K/DEN numbers are not applicable as the Predicate Devices are not identified as part of the K/DEN system.
DePuy Pinnacle™ Acetabular System, Summit™ Acetabular System, DePuy Duraloc® Cementless Acetabular Cup System, DePuy Duraloc® Cementless Acetabular Cup System, Marathon™ Cross-Linked Polyethylene Acetabular Cup Liners 36mm, Marathon™ +4 Polyethylene Liners, Modified DePuy Acetabular System
No
The description focuses on the mechanical components and materials of a hip replacement system, with no mention of AI or ML technologies.
Yes
The device is a total hip arthroplasty system intended to provide increased patient mobility and reduce pain by replacing a damaged hip joint, which are therapeutic outcomes.
No
The device is a hip implant system (Pinnacle™ Revision System) intended for total hip arthroplasty to replace damaged hip joint articulation. It is a therapy device, not a diagnostic one.
No
The device description clearly details physical components made of titanium alloy and UHMWPE, which are hardware. The intended use also describes a surgical implant.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is for replacing a damaged hip joint articulation in patients. This is a surgical procedure performed in vivo (within the body).
- Device Description: The description details the physical components of a hip implant (shell, liner, screws, etc.) and how they are used in surgery.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (blood, tissue, etc.) in vitro (outside the body) to provide information about a patient's health.
IVD devices are used to perform tests on samples taken from the body to diagnose, monitor, or screen for diseases or conditions. This device is a surgical implant used to physically replace a damaged joint.
N/A
Intended Use / Indications for Use
Total Hip Arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where is evidence of sufficient sound bone to seat and support the components. The Pinnacle Revision System is intended to be used to resurface the Acetabular socket in cementless total hip arthroplasty.
The Pinnacle" Revision System is indicated for total hip replacement in the following conditions:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, l. rheumatoid arthritis, or congenital hip dysplasia.
- Avaseular necrosis of the femoral head. 2.
- Acute traumatic fracture of the femoral head or neck. 3.
- Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, 4. hemiarthroplasty, surface replacement arthroplasty, or total hip replacement.
-
- Certain cases of ankylosis.
The Pinnacle™ Revision System Porocoat® porous-coated Acetabular Cup Shell components arc indicated for cementless application.
Product codes
87 LPH, LPI
Device Description
The Pinnacle™ Revision System is a modular system for resurfacing the acetabulum in total hip arthroplasty. It is a line extension of the DePuy Pinnacle™ Acetabular System. The system consists of two separate units, a shell and a liner. The shell substrate is manufactured from forged or wrought titanium alloy (Ti-6AL-4V). The outer porous-coating (Porocoat®) consists of commercially pure titanium beads metallurgically bonded to the shell substrate. The interior of the shell is designed to mate with a variety of styles of liners that lock into the liner is manufactured from Ultra-high molecular weight polyethylene (UHMWPE). The liners contain multiple ARDs (anti-rotation devices) that engage mating shell features to prevent rotation within the shell. The ARDs enable variable rotational alignment of Face Changing (+4 / 10°) and Lipped liners for patient appropriate positioning. The acetabular liner articulates with a compatible femoral head of appropriate diameter.
The Pinnacle™ Revision System extends the existing Pinnacle™ Acetabular System shell options by providing Multihole, Standard Profile and DPx (Deep Profile) configurations. The Revision DPx Shells provide lateralization of the femoral head. Both Revision Standard Profile and Revision DPx shells provide peripheral screw holes in addition to dome screw holes. The screw holes permit use of compatible titanium alloy screws to provide immediate adjunct fixation, stability and intimate contact with bone. The shells contain an apical threaded hole to attach the shell insertion instrument and grasp the shell during implantation. An optional titanium alloy (Ti-6Al-4V) apical hole plug is available to screw into the threaded apical hole of the shell.
The Pinnacle™ Revision System extends the range of Pinnacle™ Marathon Liners by offering corresponding sizes for 28, 32 and 36mm femoral heads in Neutral, +4, and +4 / 10' degree configurations and a Lipped liner configuration for 28 and 32mm femoral heads.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Acetabulum, femoral head, 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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
DePuy Pinnacle™ Acetabular System, Summit™ Acetabular System, DePuy Duraloc® Cementless Acetabular Cup System, DePuy Duraloc® Cementless Acetabular Cup System, Marathon™ Cross-Linked Polyethylene Acetabular Cup Liners 36mm, Marathon™ +4 Polyethylene Liners, Modified DePuy Acetabular System
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
JAN - 8 2004
033338
page 1 of 2
510(k) Summary NAME OF SPONSOR: DePuy Orthopaedics, Inc. 700 Orthopaedic Drive Warsaw, Indiana 46581-0988 Est. Reg. No. 1818910 510(K) CONTACT: Bob Friddle, BSMF Consultant, Regulatory Affairs Telephone: (574) 371-4925 Fax: (574) 371-4987 DATE PREPARED: November 18, 2003 TRADE NAME: PinnacleTM Revision System COMMON NAME: Acetabular Cup Prosthesis CLASSIFICATION: Class II Device per 21 CFR 888.3358: Hip joint metal/polymer/metal semiconstrained porous coated uncemented prosthesis DEVICE PRODUCT CODE: 87 LPH SUBSTANTIALLY EQUIVALENT DePuy Pinnacle™ Acetabular System DEVICES: Summit™ Acetabular System DePuy Duraloc® Cementless Acetabular Cup System DePuy Duraloc® Cementless Acetabular Cup System Marathon™ Cross-Linked Polyethylene Acetabular Cup Liners 36mm Marathon™ +4 Polyethylene Liners Modified DePuy Acetabular System
DEVICE DESCRIPTION:
The Pinnacle™ Revision System is a modular system for resurfacing the acetabulum in total hip arthroplasty. It is a line extension of the DePuy Pinnacle™ Acetabular System. The system consists of two separate units, a shell and a liner. The shell substrate is manufactured from forged or wrought titanium alloy (Ti-6AL-4V). The outer porous-coating (Porocoat®) consists of commercially pure titanium beads metallurgically bonded to the shell substrate. The interior of the shell is designed to mate with a variety of styles of liners that lock into the liner is manufactured from Ultra-high molecular weight polyethylene (UHMWPE). The liners contain multiple ARDs (anti-rotation devices) that engage mating shell features to prevent rotation within the shell. The ARDs enable variable rotational alignment of Face Changing (+4 / 10°) and Lipped liners for patient appropriate positioning. The acetabular liner articulates with a compatible femoral head of appropriate diameter.
1
033338
page 2 of 2
510(k) Summary (cont.)
The Pinnacle™ Revision System extends the existing Pinnacle™ Acetabular System shell options by providing Multihole, Standard Profile and DPx (Deep Profile) configurations. The Revision DPx Shells provide lateralization of the femoral head. Both Revision Standard Profile and Revision DPx shells provide peripheral screw holes in addition to dome screw holes. The screw holes permit use of compatible titanium alloy screws to provide immediate adjunct fixation, stability and intimate contact with bone. The shells contain an apical threaded hole to attach the shell insertion instrument and grasp the shell during implantation. An optional titanium alloy (Ti-6Al-4V) apical hole plug is available to screw into the threaded apical hole of the shell.
The Pinnacle™ Revision System extends the range of Pinnacle™ Marathon Liners by offering corresponding sizes for 28, 32 and 36mm femoral heads in Neutral, +4, and +4 / 10' degree configurations and a Lipped liner configuration for 28 and 32mm femoral heads.
INTENDED USE AND INDICATIONS:
Total Hip Arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. The Pinnacle Revision System is intended to be used to resurface the Acetabular socket in cementless total hip arthroplasty.
The Pinnacle™ Revision System is indicated for total hip replacement in the following conditions:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, 1.
- rheumatoid arthritis, or congenital hip dysplasia.
-
- Avascular necrosis of the femoral head.
-
- Acute traumatic fracture of the femoral head or neck.
- Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, 4. hemiarthroplasty, surface replacement arthroplasty, or total hip replacement.
- ಳ Certain cases of ankylosis.
The Pinnacle™ Revision System Acetabular Cup Shell components are indicated for cementless application.
BASIS OF SUBSTANTIAL EQUIVALENCE:
Based on the same Intended Use, Indications for Use, materials, sterilization processes and similarities of technological and geometric features, DePuy believes that the subject Pinnacle™ Revision System components are substantially equivalent to the previously cleared DePuy predicate devices.
2
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of an eagle or bird-like figure with three legs, representing the department's mission related to health and human services.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
JAN - 8 2004
Ms. Natalie Heck Manager, Regulatory Affairs DePuy Orthopaedics, Inc. P.O. Box 988 700 Orthopaedic Drive Warsaw, Indiana 46581-0988
Re: K033338 Trade/Device Name: Pinnacle™ Revision System Regulation Number: 21 CFR 888.3358 Regulation Name: Hip joint metal/polymet/metal semi-constrained porous-coated uncemented prosthesis Regulatory Class: II Product Code: LPI Dated: December 11, 2003 Received: December 12, 2003
Dear Ms. Heck:
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 Mcdical 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 may of bather to saterial 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 (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. Natalie Heck
This letter will allow you to begin marketing your device as described in your Section 510(k) This lotter will anow yourse ough finding of substantial equivalence of your device to a legally premantee notification "The 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 If you desire specific acrioliance 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 other general miorination of Journer 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,
Sincerely yours,
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
510(k) Number (if known): Device Name: Pinnacle™ Revision System
Intended Use/Indications for Use
Total Hip Arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where is evidence of sufficient sound bone to seat and support the components. The Pinnacle Revision System is intended to be used to resurface the Acetabular socket in cementless total hip arthroplasty.
The Pinnacle" Revision System is indicated for total hip replacement in the following conditions:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, l. rheumatoid arthritis, or congenital hip dysplasia.
- Avascular necrosis of the femoral head. 2.
- Acute traumatic fracture of the femoral head or neck. 3.
- Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, 4. hemiarthroplasty, surface replacement arthroplasty, or total hip replacement.
-
- Certain cases of ankylosis.
The Pinnacle™ Revision System Porocoat® porous-coated Acetabular Cup Shell components arc indicated for cementless application.
PLEASE DO NOT WRITE BELOW THIS LINE -- CONTINUE ON ANOTHER PAGE IF NEEDED. Concurrence of CDRH, Office of Device Evaluation (ODE)
Makan melkeran
for K033338
ision Sign-Off)
ision of General, Restorative
Neurological Devices
Number
K0553
Prescription Use X OR Over-The-Counter Use
(Per 21 CFR 801.109)