(123 days)
No
The 510(k) summary describes a mechanical shoulder implant system and does not mention any AI or ML components or functionalities.
Yes
This device is a shoulder joint replacement system used to treat conditions like arthritis and fractures, aiming to restore function and alleviate pain. These are therapeutic actions.
No
Explanation: The device is a shoulder replacement system, which is an orthopedic implant used to treat conditions like arthritis and fractures, not to diagnose them.
No
The device description clearly outlines physical components (Modular Distal Stem, Modular Anatomic Metaphysis, Modular Anatomic Assembly Screw) that are assembled in the operating room, indicating it is a hardware device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is a replacement for shoulder joints disabled by various conditions. This is a surgical implant, not a device used to perform tests on samples taken from the body (like blood, urine, or tissue).
- Device Description: The description details the components of a shoulder implant system that is assembled and used in the operating room.
- Lack of IVD Characteristics: There is no mention of analyzing biological samples, detecting substances, or providing diagnostic information based on in vitro testing.
IVD devices are used to examine specimens derived from the human body to provide information for diagnostic, monitoring, or compatibility purposes. This device is a prosthetic implant used to restore function to a damaged joint.
N/A
Intended Use / Indications for Use
The Aequalis Ascend Modular Anatomic Shoulder System is indicated for use as a replacement of Shoulder joints disabled by:
- Rheumatoid arthritis with pain O
- Non-inflammatory degenerative joint disease (i.e. osteoarthritis and o avascular necrosis)
- Correction of functional deformity O
- Fractures of the humeral head O
- Traumatic arthritis 0
Notes:
- All components are single use
- The humeral stem is intended for cemented or cementless use
- The glenoid component is intended for cemented use .
Product codes
HSD, KWT, KWS
Device Description
The Aequalis Ascend Modular Anatomic Shoulder system is a modular version of the Ascend Monolithic Shoulder System (K071147) with anatomic adapters.
The Aequalis Ascend Modular Anatomic Shoulder system is supplied in separate sterile packages which will be assembled in the operating room. The components provided will be:
- The Modular Distal Stem.
- The Modular Anatomic Metaphysis.
- The Modular Anatomic Assembly Screw.
This assembly will mate with existing; FDA cleared Tornier Ascend Monolithic Humeral Heads (K07) 147) which were designed to articulate with FDA cleared Tornier Aequalis and Affiniti Glenoid replacements (K063081 and K060988 respectively ).
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Shoulder joints / humeral head
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)
K071147, K980244, K011942, K063081, K952928, K060988, K060692
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 888.3660 Shoulder joint metal/polymer semi-constrained cemented prosthesis.
(a)
Identification. A shoulder joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a shoulder 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 humeral resurfacing component made of alloys, such as cobalt-chromium-molybdenum, and a glenoid resurfacing component made of ultra-high molecular weight polyethylene, and is limited to those prostheses intended for use with bone cement (§ 888.3027).(b)
Classification. Class II. The special controls for this device are:(1) FDA's:
(i) “Use of International Standard ISO 10993 ‘Biological Evaluation of Medical Devices—Part I: Evaluation and Testing,’ ”
(ii) “510(k) Sterility Review Guidance of 2/12/90 (K90-1),”
(iii) “Guidance Document for Testing Orthopedic Implants with Modified Metallic Surfaces Apposing Bone or Bone Cement,”
(iv) “Guidance Document for the Preparation of Premarket Notification (510(k)) Application for Orthopedic Devices,” and
(v) “Guidance Document for Testing Non-articulating, ‘Mechanically Locked’ Modular Implant Components,”
(2) International Organization for Standardization's (ISO):
(i) ISO 5832-3:1996 “Implants for Surgery—Metallic Materials—Part 3: Wrought Titanium 6-aluminum 4-vandium Alloy,”
(ii) ISO 5832-4:1996 “Implants for Surgery—Metallic Materials—Part 4: Cobalt-chromium-molybdenum casting alloy,”
(iii) ISO 5832-12:1996 “Implants for Surgery—Metallic Materials—Part 12: Wrought Cobalt-chromium-molybdenum alloy,”
(iv) ISO 5833:1992 “Implants for Surgery—Acrylic Resin Cements,”
(v) ISO 5834-2:1998 “Implants for Surgery—Ultra-high Molecular Weight Polyethylene—Part 2: Moulded Forms,”
(vi) ISO 6018:1987 “Orthopaedic Implants—General Requirements for Marking, Packaging, and Labeling,” and
(vii) ISO 9001:1994 “Quality Systems—Model for Quality Assurance in Design/Development, Production, Installation, and Servicing,” and
(3) American Society for Testing and Materials':
(i) F 75-92 “Specification for Cast Cobalt-28 Chromium-6 Molybdenum Alloy for Surgical Implant Material,”
(ii) F 648-98 “Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants,”
(iii) F 799-96 “Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Forgings for Surgical Implants,”
(iv) F 1044-95 “Test Method for Shear Testing of Porous Metal Coatings,”
(v) F 1108-97 “Specification for Titanium-6 Aluminum-4 Vanadium Alloy Castings for Surgical Implants,”
(vi) F 1147-95 “Test Method for Tension Testing of Porous Metal,”
(vii) F 1378-97 “Standard Specification for Shoulder Prosthesis,” and
(viii) F 1537-94 “Specification for Wrought Cobalt-28 Chromium-6 Molybdenum Alloy for Surgical Implants.”
0
Image /page/0/Picture/0 description: The image contains a sequence of handwritten alphanumeric characters. The characters are 'K102924'. The characters are written in a dark ink on a white background.
: . . .
SECTION 5
510(k) SUMMARY
Summary of Safety and Effectiveness information
Tornier Inc. Aequalis Ascend Modular Anatomic Shoulder System
Regulatory authority: Safe Medical Devices Act of 1990, 21 CRF 807.92
1) Device name
Aequalis Ascend Modular Anatomic Shoulder System Trade name: Common name: Shoulder Prosthesis Classification Number/ Classification name/Product code:
- . Shoulder joint, humeral (hemi-Shoulder), metallic uncemented prosthesis are class II devices under 21 CFR 888.3690 (product code HSD) and are classified by the Orthopedic Devices Panel.
- Shoulder joint metal/polymer non-constrained cemented prosthesis are class II . devices under 21 CFR 888.3650 (product code KWT) and are classified by the Orthopedic Devices Panel.
- Shoulder joint metal/polymer semi-constrained cemented prosthesis are class II . devices under 21 CFR 888.3660 (product code KWS) and are classified by the Orthopedic Devices Panel.
2) Submitter
- Tornier Inc.
- 7701 France Avenue South; Suite 600
- Edina, MN 55435
Registration Number: 9100540
3) Company contact
Brahim Hadri
Sr. Regulatory affairs Specialist 100 Cummings Center, Suite 444C, Beverly, MA 01915, U.S.A Phone: 1 978 232-9997 ext: 617 1 978-232-9998 Fax: bhadri@tornier.com
1
-
- Classification Device class: Classification panel: Product code:
Class II Orthopedic HSD: KWT: KWS
- Classification Device class: Classification panel: Product code:
5) Legally Marketed Device to which Equivalence is Claimed:
- · Tornier Nexa Orthopedics Total Shoulder System: K071147
- · Tornier Aequalis Shoulder Prosthesis: K980244, K011942, K063081, K952928
- · Tornier DVO Total and Hemi Shoulder System: K060988
- · Biomet Comprehensive Primary Shoulder Stems: K060692
Notes:
- The Tornier Nexa Orthopedics Total Shoulder System (K071147) is presently named . Ascend Monolithic Shoulder System and hereafter will be referred to as such.
- The Tornier DVO Total and Hemi Shoulder System (K060988) is presently named . Affiniti Shoulder System and hereafter will be referred to as such.
6) Device description
The Aequalis Ascend Modular Anatomic Shoulder system is a modular version of the Ascend Monolithic Shoulder System (K071147) with anatomic adapters.
The Aequalis Ascend Modular Anatomic Shoulder system is supplied in separate sterile packages which will be assembled in the operating room. The components provided will be:
- . The Modular Distal Stem.
- . The Modular Anatomic Metaphysis.
- . The Modular Anatomic Assembly Screw.
This assembly will mate with existing; FDA cleared Tornier Ascend Monolithic Humeral Heads (K07) 147) which were designed to articulate with FDA cleared Tornier Aequalis and Affiniti Glenoid replacements (K063081 and K060988 respectively ).
2
7) Materials
- The Modular Distal Stem and Modular Anatomic Metaphysis components are manufactured from . Titanium according to ASTM F 136 Standard Specification for Wrought Titanium - 6Aluminum -4 Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications
- . The Modular Anatomic Assembly Screw is manufactured from Cobalt Chromium Molybdenum allov according to ASTM F-1537 Standard Specification for Wrought Cobalt-28-Chromium-6-Molybdenum Alloy for Surgical Implants
- . The Modular Anatomic Assembly Screw includes an Ultra High Molecular Weight Polyethylene (UHMWPE) plug to prevent loosening. The material of the screw is accordance to ASTM F648 Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants or ISO-5834-2. Implants for surgery -- Ultra-highmolecular-weight polyethylene -- Part 2: Moulded forms
8} Indications for Use
- . The Aequalis Ascend Modular Anatomic Shoulder System is indicated for use as a replacement of Shoulder joints disabled by:
- Rheumatoid arthritis with pain o
- Non-inflammatory degenerative joint disease (i.e. osteoarthritis and avascular o necrosis)
- Correction of functional deformity o
- Fractures of the humeral head o
- Traumatic arthritis O
Notes:
- All components are single use .
- . The humeral stem is intended for cemented or cementless use
- The glenoid component is intended for cemented use .
9) Summary of technologies
The technological characteristics (material, design, sizing, indications) of the Tornier Aequalis Ascend Modular Anatomic Shoulder System are similar or identical to the cited predicate devices.
3
Image /page/3/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo features a stylized eagle with three stripes forming its body and wings. The eagle is facing right. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged in a circular fashion around the eagle.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Tornier Inc. % Mr. Brahim Hadri Senior Regulatory Affairs Specialist 7701 France Ave South; Suite 600 Edina, Minnesota 55435
JAN 3 1 201
Re: K102924
Trade/Device Name: Aequalis® Ascend™ Modular Anatomic Shoulder System Regulation Number: 21 CFR 888.3660 Regulation Name: Shoulder joint metal/polymer semi-constrained cemented prosthesis Regulatory Class: Class II Product Code: KWS, KWS, KWT, HSD Dated: January 12, 2011 Received: January 12, 2011
Dear Mr. Hadri:
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, Orug 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 (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
4
Page 2 – Mr. Brahim Hadri
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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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,
A.J. B. R.
for.
Mark N. Melkerson Director Division of Surgical, Orthopedic, and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
5
Indications for Use
510(k) Number (if known):
Device Name: Aequalis® Ascend™ Modular Anatomic Shoulder System
Indications for Use
- . The Aequalis Ascend Modular Anatomic Shoulder System is indicated for use as a replacement of Shoulder joints disabled by:
- Rheumatoid arthritis with pain O
- Non-inflammatory degenerative joint disease (i.e. osteoarthritis and o avascular necrosis)
- Correction of functional deformity O
- Fractures of the humeral head O
- Traumatic arthritis 0
Notes:
- . All components are single use
- . The humeral stem is intended for cemented or cementless use
- The glenoid component is intended for cemented use .
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 NECESSARY) Concurrence of CDRH, Office of Device Evaluation (ODE)
Nilfredohn for mxm
(Division Sign Off)
Division of Surgical, Orthopedic, and Restorative Devices
510(k) Number: K102924