(28 days)
No
The summary describes a mechanical hip implant system and does not mention any software, algorithms, or capabilities related to AI or ML. The changes described are physical modifications to existing components.
Yes
The device is a component of a total hip replacement system, which is used to treat severely painful and/or disabled joints, acute traumatic fractures, and failed previous hip surgeries, thus providing a therapeutic benefit to the patient.
No
Explanation: The device is a total hip replacement system, indicated for surgical use to replace a hip joint. While it includes features for measuring implant migration post-surgery, its primary function is therapeutic replacement, not diagnosing conditions.
No
The device description clearly outlines physical components (femoral stem, acetabular shell, tantalum beads, screw hole occluders) which are hardware.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or screening.
- Device Description: The PIPELINE Total Hip System is a physical implant designed to replace a damaged hip joint. It is surgically implanted into the patient's body.
- Intended Use: The intended use clearly describes a surgical procedure for total hip replacement, not the analysis of biological samples.
The device is a surgical implant, not a diagnostic tool that analyzes samples outside of the body.
N/A
Intended Use / Indications for Use
The PIPELINE Total Hip System is indicated for use in skeletally mature individuals undergoing surgery for total hip replacement due to:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid . arthritis, avascular necrosis, or congenital hip dysplasia.
- . Acute traumatic fracture of the femoral head or neck.
- Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, ● hemiarthroplasty, surface replacement arthroplasty or total hip replacement.
The PIPELINE Tapered Femoral Stem and PIPELINE PST™ Acetabular Shell are intended for cementless or cemented fixation. The porous structured surface provides biological fixation when used in a cementless application.
The PIPELINE PST™ Acetabular Shell with HA is intended for cementless fixation. The porous structured surface with HA provides biological fixation.
Product codes
LPH, JDI, OQG, OQH, LZO, OQI, MEH
Device Description
This 510(k) addresses the addition of the following components (already cleared under 510(k) #K130353) to the subject hip system:
- . A size 1 femoral stem;
- Hip stems (all sizes, 1-12) with the option of 3 tantalum beads, to allow the surgeon to perform . radiostereometric analysis(RSA) to measure implant migration; and
- . Optional acetabular screw hole occluders provided either separately (for assembly by the surgeon), or pre-assembled to the acetabular shells.
These components are compatible with the total hip system determined substantially equivalent as the Pipeline Total Hip System in 510(k) #K12802 and K131237 and as the PBP Total Hip System in 510(k) #K122158.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Hip
Indicated Patient Age Range
skeletally mature individuals
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)
The subject devices are identical in every aspect to the predicate devices cleared through 510(k) #K130353. The only change being made is to the Pipeline Biomedical Holdings subsidiary name assigned to the 510(k). Therefore, no additional testing was conducted.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
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
510(k) Summary - 510(k) #K132626
The following 510(k) Summary is provided in accordance with the requirements of 21 CFR 807.92.
| Device Name and Classification | |
|---|---|
| Device Trade Name: | Pipeline Total Hip System - Line Extension |
| Device Common Name: | Artificial Total Hip Replacement |
| Regulation Number and Description: | 888.3358 - Hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis |
| Device Class: | II |
| Product Codes: | LPH - prosthesis, hip, semi-constrained, metal/polymer, porous uncemented |
| JDI - prosthesis, hip, semi-constrained, metal/polymer, cemented | |
| OQG - hip prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented | |
| OQH - hip, semi-constrained, cemented, metal/polymer + additive, cemented | |
| LZO (Hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis) | |
| OQI (hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented) | |
| MEH (prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calcium-phosphate) | |
| Advisory Panel: | Orthopedic |
| Address and Registration | |
| Submitter's Name: | Pipeline Biotechnology, LLC |
| Submitter's Name: | Pipeline Biotechnology, LLC |
|---|---|
| Address: | 3 Wing Drive Suite 102 Cedar Knolls, NJ 07927 |
| Contact Person: | Jaclyn C. Docs |
| Telephone Number: | (973) 267-8800 |
| Fax Number: | (973) 267-8810 |
| Date Summary Prepared: | August 21, 2013 |
| Establishment Registration Number: | Not registered yet |
Purpose of Submission
This Special 510(k) addresses an administrative line extension to the subject total hip system (510(k) #K122158), and introduces hip system components that have already been determined substantially equivalent by FDA in 510(k) #K130353 for the designated indications for use under the name of another subsidiary of the parent holding company.
Identification of Legally Marketed Device to which Submitter Claims Equivalence
The subject size #1 hip stems, RSA hip stems, and acetabular shell screw hole occluder submitted in this
1
510(k) under the name of Pipeline Biotechnology, are identical, and therefore substantially equivalent to, the same devices cleared under the name of Pipeline Biomedical Holdings' subsidiary, Pipeline Orthopedics, in predicate 510(k) number K130353.
Device Description
This 510(k) addresses the addition of the following components (already cleared under 510(k) #K130353) to the subject hip system:
- . A size 1 femoral stem;
- Hip stems (all sizes, 1-12) with the option of 3 tantalum beads, to allow the surgeon to perform . radiostereometric analysis(RSA) to measure implant migration; and
- . Optional acetabular screw hole occluders provided either separately (for assembly by the surgeon), or pre-assembled to the acetabular shells.
These components are compatible with the total hip system determined substantially equivalent as the Pipeline Total Hip System in 510(k) #K12802 and K131237 and as the PBP Total Hip System in 510(k) #K122158.
Intended Use
The PIPELINE Total Hip System is indicated for use in skeletally mature individuals undergoing surgery for total hip replacement due to:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid . arthritis, avascular necrosis, or congenital hip dysplasia.
- . Acute traumatic fracture of the femoral head or neck.
- Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, ● hemiarthroplasty, surface replacement arthroplasty or total hip replacement.
The PIPELINE Tapered Femoral Stem and PIPELINE PST™ Acetabular Shell are intended for cementless or cemented fixation. The porous structured surface provides biological fixation when used in a cementless application.
The PIPELINE PST™ Acetabular Shell with HA is intended for cementless fixation. The porous structured surface with HA provides biological fixation.
Comparison of Technological Characteristics
The components described in this 510(k) are identical to the same components determined substantially equivalent in predicate 510(k) #K130353 in all respects except for the Pipeline Biomedical Holdings subsidiary name assigned to the 510(k). There is no difference in intended use, materials, design features, component sizing, or manufacturing methods.
Summary of Nonclinical Testing
The subject devices are identical in every aspect to the predicate devices cleared through 510(k) #K130353. The only change being made is to the Pipeline Biomedical Holdings subsidiary name assigned to the 510(k). Therefore, no additional testing was conducted.
Conclusions
The subject components share the same indications for use as the predicate components, and feature the identical design, materials, sizing, manufacturing/packaging/sterilization methods and performance characteristics, and are therefore substantially equivalent.
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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized depiction of a human figure with outstretched arms, symbolizing care and protection. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES (USA)" is arranged in a circular pattern around the figure. The logo is presented in black and white.
Food and Drug Administration 0903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
October 16, 2013
Pipeline Biotechnology, LLC % Ms. Terry Sheridan Powell M Squared Associates Incorporated, Consultants for Pipeline Biotechnology, LLC. 575 Eighth Avenue, Suite 1212 New York, New York 10018
Re: K132626
Trade/Device Name: Pipeline Total Hip System 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, JDI, OQG, OQH, LZO, OQI, MEH Dated: August 21, 2013 Received: August 22, 2013
Dear Ms. Powell:
This letter corrects our substantially equivalent letter of September 19, 2013.
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
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Page 2 - Ms. Terry Sheridan Powell
comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807): labeling (21 CFR Part 801): medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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 advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree 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 Small Manufacturers, International and Consumer Assistance 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.
Erin Keith
for
Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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б Indication for Use Statement
510(k) Number (if known); K 132626 to be assigned
PIPELINE Total Hip System is indicated for use in skeletally mature individuals undergoing surgery for total hip replacement due to:
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, . rheumatoid arthritis, avascular necrosis, or congenital hip dysplasia;
- . Acute traumatic fracture of the femoral head or neck;
- . Failed previous hip surgery including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty or total hip replacement.
The PIPELINE Tapered Femoral Stem and PIPELINE PST™ Acetabular Shell are intended for cementless or cemented fixation. The porous structured surface provides biological fixation when used in a cementless application.
The PIPELINE PST™ Acetabular Shell with HA is intended for cementless fixation. The porous structured surface with HA provides biological fixation.
x Prescription Use AND/OR (Part 21 CFR 801 Subpart D)
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)
Elizabeth L. Frank -S
Page 1 of ____________________________________________________________________________________________________________________________________________________________________
CONFIDENTIAL