(152 days)
Not Found
No
The device description and intended use indicate that this is a mechanical implant (suture anchor) and does not mention any software, image processing, or AI/ML capabilities.
Yes.
Explanation: The device is described as an implantable anchor designed to secure soft tissue to bone for various repairs and reconstructions, such as rotator cuff repair and ACL repair. These applications are for treating or preventing disease or affecting the structure or function of the body, which aligns with the definition of a therapeutic device.
No
The device is an anchor designed to secure soft tissue to bone, used for repair and reconstruction, rather than for diagnosing conditions.
No
The device description clearly states that the devices are "implantable cannulated, threaded anchors" made of physical materials (Biocryl Rapide, PEEK, etc.) and are provided with physical components like inserter shafts and stay sutures. This indicates a hardware medical device, not a software-only one.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens (like blood, urine, or tissue) taken from the human body to provide information for diagnosis, monitoring, or screening.
- Device Description: The description clearly states that the HEALIX ADVANCE anchors are "implantable cannulated, threaded anchors designed to secure soft tissue to bone utilizing suture". They are physical devices implanted into the body during surgery.
- Intended Use: The intended uses listed are all surgical procedures to repair or reconstruct ligaments and tendons in various joints (shoulder, elbow, knee, foot, and ankle). These are direct surgical interventions, not diagnostic tests performed on specimens outside the body.
The text describes a surgical implant used for musculoskeletal repair, which falls under the category of medical devices, but specifically not In Vitro Diagnostics.
N/A
Intended Use / Indications for Use
HEALIX ADVANCE Knotless anchors: The DePuy Mitek HEALIX ADVANCE Knotless BR anchors is indicated as follows: - · Shoulder: Rotator Cuff Repair - · Shoulder: Bicep Tenodesis - · Shoulder: Deltoid Repair - · Elbow: Ulnar Collateral Ligament (UCL) - · Elbow: Radial Collateral Ligament (RCL) - · Knee: Posterior Oblique - · Knee: Medial Collateral Ligament (MCL) - · Knee: Lateral Collateral Ligament (LCL) - · Knee: Iliotibial (IT) Band Tenodesis - · Knee: Anterior Cruciate Ligament (ACL) Repair - · Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair - · Knee: Meniscal Root Repair - · Foot and Ankle: Achilles Tendon Repair The DePuy Mitek HEALIX ADVANCE KNOTLESS PEEK Anchors is indicated as follows: - · Shoulder: Rotator Cuff Repair - · Shoulder: Bicep Tenodesis - · Shoulder: Deltoid Repair - · Elbow: Ulnar Collateral Ligament (UCL) - · Elbow: Radial Collateral Ligament (RCL) - · Knee: Posterior Oblique - · Knee: Medial Collateral Ligament (MCL) - · Knee: Lateral Collateral Ligament (LCL) - · Knee: Iliotibial (IT) Band Tenodesis - · Knee: Anterior Cruciate Ligament (ACL) Repair - · Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair - · Knee: Meniscal Root Repair - · Foot and Ankle: Achilles Tendon Repair - · Foot and Ankle: Lateral Stabilization - · Foot and Ankle: Medial Stabilization HEALIX ADVANCE Self-Punching anchors: The DePuy Mitek HEALIX ADVANCE SP Biocomposite Anchors is indicated as follows: - · Shoulder: Rotator Cuff Repair - · Shoulder: Bicep Tenodesis - Shoulder: Deltoid Repair - Elbow: Ulnar Collateral Ligament (UCL) - Elbow: Radial Collateral Ligament (RCL) - Knee: Posterior Oblique - Knee: Medial Collateral Ligament (MCL) - Knee: Lateral Collateral Ligament (LCL) - Knee: Iliotibial (IT) Band Tenodesis - Knee: Anterior Cruciate Ligament (ACL) Repair - Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair - Knee: Meniscal Root Repair The DePuy Mitek HEALIX ADVANCE SP PEEK Anchors is indicated as follows: - Shoulder: Rotator Cuff Repair - Bicep Tenodesis Deltoid Repair Elbow Ulnar Collateral Ligament (UCL) reconstruction Radial Collateral Ligament (RCL) reconstruction Knee Posterior Oblique repair Medial Collateral Ligament (MCL) reconstruction Lateral Collateral Ligament reconstruction Iliotibial (IT) Band Tenodesis Anterior Cruciate Ligament (ACL) Repair Secondary Fixation in ACL/PCL Reconstruction/Repair Meniscal Root Repair Foot/Ankle Achilles Tendon Repair Lateral Stabilization Medial Stabilization
Product codes (comma separated list FDA assigned to the subject device)
MAI, MBI
Device Description
The subject devices of this Special 510(k) are the HEALIX ADVANCE Knotless anchors and HEALIX ADVANCE Self-Punching (SP) anchors. The HEALIX ADVANCE Knotless Anchor is a one-piece implantable cannulated, threaded anchor designed to secure soft tissue to bone utilizing suture (provided separately). The anchor is preloaded on a disposable inserter shaft with handle, held in place by a #2 ORTHOCORD stay suture comprised of Ultra-High Molecular Weight Polyethylene (UHMWPE) and violet Polydioxanone (PDS). During implantation, the stay suture may be discarded or incorporated into the repair at the surgeon's discretion. The anchor is provided preloaded on a single-use driver. The anchor is offered in three sizes: 4.75mm, 5.5mm and 6.5mm. The anchors are available in two materials: Biocryl Rapide® (BR) and Polyetheretherketone (PEEK) materials. The Biocryl Rapide material is a biocomposite material of 70% PLGA copolymer (85% PLLA/15% PGA) and 30% β-TCP. The HEALIX ADVANCE KNOTLESS Anchor is provided sterile and is for single use only. The HEALIX ADVANCE SP Anchor is a two-piece "self-punching" design consisting of a cannulated, threaded anchor and dilator designed to secure soft tissue to bone utilizing suture (provided separately). The anchor-dilator are preloaded on a disposable inserter shaft with handle, held in place by a non-absorbable stay suture comprised of Ultra-High Molecular Weight Polyethylene (UHMWPE) and Green poly (ethylene terephthalate) (PET). During implantation, the stay suture may be discarded or incorporated into the repair at the surgeon's discretion. The HEALIX ADVANCE SP Anchor is offered in three sizes: 4.9mm, 5.5mm and 6.5mm. The anchors are available in two materials: Biocomposite (Biocryl) and Polyetheretherketone (PEEK) material. Biocryl is an absorbable biocomposite of Polylactic Acid (PLA) and Tricalcium Phosphate (TCP). The HEALIX ADVANCE SP Anchor is provided sterile and is for single use only.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Shoulder, Elbow, Knee, Foot and Ankle
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: Verification activities were performed on the proposed device. Verification included an assessment of fixation strength for proposed indications at T=0 and over the healing period, as well as assessment of insertion force. Safety and Performance: Results of the analyses demonstrated that the devices continue to meet established design inputs and corresponding criteria, and that there were no new issues of safety or effectiveness related to device performance. Based on similarities in the intended use, technological characteristics, and performance in comparison to the predicate devices, the modified HEALIX ADVANCE Knotless anchors and HEALIX ADVANCE Self-Punching anchors have shown to be substantially equivalent to the predicate devices under the Federal Food, Drug and Cosmetic Act.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
K180101, K171114, K191242, K182941, K201883
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 888.3030 Single/multiple component metallic bone fixation appliances and accessories.
(a)
Identification. Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.(b)
Classification. Class II.
0
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September 11, 2024
DePuy Mitek Lidia Moses Regulatory Affairs Specialist II 325 Paramount Drive Raynham, Massachusetts 02767
Re: K241010
Trade/Device Name: HEALIX ADVANCE Knotless anchors; HEALIX ADV ANCE Self-Punching anchors Regulation Number: 21 CFR 888.3030 Regulation Name: Single/Multiple Component Metallic Bone Fixation Appliances And Accessories Regulatory Class: Class II Product Code: MAI, MBI Dated: April 12, 2024 Received: September 9, 2024
Dear Lidia Moses:
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 (the 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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrb/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.
1
Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).
Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).
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 of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.
All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-device-advicecomprehensive-regulatory-assistance/unique-device-identification-system-udi-system.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
2
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn
(https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Thomas Mcnamara -S
For: Christopher Ferreira, MS Assistant Director DHT6C: Division of Restorative, Repair, and Trauma Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
3
Indications for Use
Submission Number (if known)
Device Name
HEALIX ADVANCE Knotless anchors;
HEALIX ADVANCE Self-Punching anchors
Indications for Use (Describe)
HEALIX ADVANCE Knotless anchors:
The DePuy Mitek HEALIX ADVANCE Knotless BR anchors is indicated as follows:
- · Shoulder: Rotator Cuff Repair
- · Shoulder: Bicep Tenodesis
- · Shoulder: Deltoid Repair
- · Elbow: Ulnar Collateral Ligament (UCL)
- · Elbow: Radial Collateral Ligament (RCL)
- · Knee: Posterior Oblique
- · Knee: Medial Collateral Ligament (MCL)
- · Knee: Lateral Collateral Ligament (LCL)
- · Knee: liotibial (IT) Band Tenodesis
- · Knee: Anterior Cruciate Ligament (ACL) Repair
- · Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair
- · Knee: Meniscal Root Repair
- · Foot and Ankle: Achilles Tendon Repair
The DePuy Mitek HEALIX ADVANCE KNOTLESS PEEK Anchors is indicated as follows:
- · Shoulder: Rotator Cuff Repair
- · Shoulder: Bicep Tenodesis
- · Shoulder: Deltoid Repair
- · Elbow: Ulnar Collateral Ligament (UCL)
- · Elbow: Radial Collateral Ligament (RCL)
- · Knee: Posterior Oblique
- · Knee: Medial Collateral Ligament (MCL)
- · Knee: Lateral Collateral Ligament (LCL)
- · Knee: liotibial (IT) Band Tenodesis
- · Knee: Anterior Cruciate Ligament (ACL) Repair
- · Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair
- · Knee: Meniscal Root Repair
- · Foot and Ankle: Achilles Tendon Repair
- · Foot and Ankle: Lateral Stabilization
- · Foot and Ankle: Medial Stabilization
HEALIX ADVANCE Self-Punching anchors:
The DePuy Mitek HEALIX ADVANCE SP Biocomposite Anchors is indicated as follows:
- · Shoulder: Rotator Cuff Repair
- · Shoulder: Bicep Tenodesis
Form Approved: OMB No. 0910-0120 Expiration Date: 07/31/2026 See PRA Statement below.
4
| • Shoulder: Deltoid Repair |
|---|
| • Elbow: Ulnar Collateral Ligament (UCL) |
| • Elbow: Radial Collateral Ligament (RCL) |
| • Knee: Posterior Oblique |
| • Knee: Medial Collateral Ligament (MCL) |
| • Knee: Lateral Collateral Ligament (LCL) |
| • Knee: liotibial (IT) Band Tenodesis |
| • Knee: Anterior Cruciate Ligament (ACL) Repair |
| • Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair |
| • Knee: Meniscal Root Repair |
The DePuy Mitek HEALIX ADVANCE SP PEEK Anchors is indicated as follows:
| • Shoulder: Rotator Cuff Repair |
|---|
| • Shoulder: Bicep Tenodesis |
| • Shoulder: Deltoid Repair |
| • Elbow: Ulnar Collateral Ligament (UCL) |
| • Elbow: Radial Collateral Ligament (RCL) |
| • Knee: Posterior Oblique |
| • Knee: Medial Collateral Ligament (MCL) |
| • Knee: Lateral Collateral Ligament (LCL) |
| • Knee: liotibial (IT) Band Tenodesis |
| • Knee: Anterior Cruciate Ligament (ACL) Repair |
| • Knee: Secondary Fixation in ACL/PCL Reconstruction/Repair |
| • Knee: Meniscal Root Repair |
| • Foot and Ankle: Achilles Tendon Repair |
| • Foot and Ankle: Lateral Stabilization |
| • Foot and Ankle: Medial Stabilization |
Type of Use (Select one or both, as applicable)
Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
CONTINUE ON A SEPARATE PAGE IF NEEDED.
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DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
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510(k) Summary
HEALIX ADVANCE™ Knotless Anchors, HEALIX ADVANCE™ Self-Punching Anchors
Date Prepared: 04/12/2024
| Submitter's Name and Address | DePuy Synthes Mitek Sports Medicine
a Johnson & Johnson company
325 Paramount Drive
Raynham, MA 02767
On behalf of:
Medos International SARL
Chemin-Blanc 38, Le Locle Neuchatel
CH 2400, Switzerland |
|------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Contact Person | Lidia Moses
Regulatory Affairs Specialist II, Regulatory Affairs
DePuy Synthes Mitek Sports Medicine
a Johnson & Johnson company
325 Paramount Drive
Raynham, MA 02767 |
| | Telephone: 508-405-7569
Email: lmoses@its.jnj.com |
| Name of Medical Device | Proprietary Name:
A) HEALIX ADVANCE™ KNOTLESS BR Anchor
B) HEALIX ADVANCE™ KNOTLESS PEEK Anchor
C) HEALIX ADVANCE™ SP BIOCOMPOSITE Anchor
D) HEALIX ADVANCE™ SP PEEK Anchor |
| | Classification Name:
A) Single/multiple component metallic bone fixation appliances and accessories
B) Smooth or threaded metallic bone fixation fastener
C) Single/multiple component metallic bone fixation appliances and accessories
D) Smooth or threaded metallic bone fixation fastener |
| | Product Code:
A) MAI
B) MBI
C) MAI
D) MBI |
| | Common Name:
Suture Anchor |
6
n & Johnson
| Substantial
Equivalence | The HEALIX ADVANCE Knotless BR anchors are substantially equivalent to predicate:
• K180101 HEALIX ADVANCE Knotless BR
The HEALIX ADVANCE Knotless PEEK anchors are substantially equivalent to predicate:
• K171114 HEALIX ADVANCE Knotless PEEK
The HEALIX ADVANCE Self-Punching Biocomposite anchors (4.9mm, 5.5mm lengths) are substantially equivalent to predicate:
• K191242 HEALIX ADVANCE Self-Punching Biocomposite anchors (4.9mm, 5.5mm lengths)
The HEALIX ADVANCE Self-Punching PEEK anchors (4.9mm, 5.5mm lengths) are substantially equivalent to predicate:
• K182941 HEALIX ADVANCE Self-Punching PEEK anchors (4.9mm, 5.5mm lengths)
The HEALIX ADVANCE Self-Punching PEEK & Biocomposite anchors 6.5mm lengths) are substantially equivalent to predicate:
• K201883 HEALIX ADVANCE Self-Punching PEEK & Biocomposite anchors (6.5mm lengths) |
|----------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Device
Classification | HEALIX ADVANCE KNOTLESS PEEK Anchor and HEALIX ADVANCE SP PEEK Anchor are classified as:
Smooth or threaded metallic bone fixation fasteners, classified as Class II, product code MBI, regulated under 21 CFR 888.3040.
HEALIX ADVANCE KNOTLESS BR Anchor and HEALIX ADVANCE SP BIOCOMPOSITE Anchor are classified as:
Single/multiple component metallic bone fixation appliances and accessories, classified as Class II, product code MAI, regulated under 21 CFR 888.3030. |
| Device Panel | Orthopedic Devices |
| Device
Description | The subject devices of this Special 510(k) are the HEALIX ADVANCE Knotless anchors and HEALIX ADVANCE Self-Punching (SP) anchors.
The HEALIX ADVANCE Knotless Anchor is a one-piece implantable cannulated, threaded anchor designed to secure soft tissue to bone utilizing suture (provided separately). The anchor is preloaded on a disposable inserter shaft with handle, held in place by a #2 ORTHOCORD stay suture comprised of Ultra-High Molecular Weight Polyethylene (UHMWPE) and violet Polydioxanone (PDS). During implantation, the stay suture may be discarded or incorporated into the repair at the surgeon's discretion. The anchor is provided preloaded on a single-use driver. The anchor is offered in three sizes: 4.75mm, 5.5mm and 6.5mm. The |
| | anchors are available in two materials: Biocryl Rapide® (BR) and
Polyetheretherketone (PEEK) materials. The Biocryl Rapide material is a
biocomposite material of 70% PLGA copolymer (85% PLLA/15% PGA) and 30%
β-TCP. The HEALIX ADVANCE KNOTLESS Anchor is provided sterile and is
for single use only. |
| | The HEALIX ADVANCE SP Anchor is a two-piece "self-punching" design
consisting of a cannulated, threaded anchor and dilator designed to secure soft
tissue to bone utilizing suture (provided separately). The anchor-dilator are
preloaded on a disposable inserter shaft with handle, held in place by a non-
absorbable stay suture comprised of Ultra-High Molecular Weight Polyethylene
(UHMWPE) and Green poly (ethylene terephthalate) (PET). During implantation,
the stay suture may be discarded or incorporated into the repair at the surgeon's
discretion. The HEALIX ADVANCE SP Anchor is offered in three sizes: 4.9mm,
5.5mm and 6.5mm. The anchors are available in two materials: Biocomposite
(Biocryl) and Polyetheretherketone (PEEK) material. Biocryl is an absorbable
biocomposite of Polylactic Acid (PLA) and Tricalcium Phosphate (TCP). The
HEALIX ADVANCE SP Anchor is provided sterile and is for single use only. |
| Technological
Characteristics | The anchor design, materials, principal of operation, and intended use of the
subject devices are identical to that of the predicate devices. This submission is
made in support of a modification to the labeling of the subject devices to add
additional indications and a modification to the suture compatibility language
within the Instructions for Use. |
| Indications for
Use | HEALIX ADVANCE Knotless anchors (Note: new indications are underlined): |
| | The DePuy Mitek HEALIX ADVANCE Knotless BR anchors is indicated as |
| | follows: |
| | Shoulder ○ Rotator Cuff Repair ○ Bicep Tenodesis ○ Deltoid Repair Elbow ○ Ulnar Collateral Ligament (UCL) ○ Radial Collateral Ligament (RCL) Knee ○ Posterior Oblique ○ Medial Collateral Ligament (MCL) ○ Lateral Collateral Ligament (LCL) ○ Iliotibial (IT) Band Tenodesis ○ Anterior Cruciate Ligament (ACL) Repair ○ Secondary Fixation in ACL/PCL Reconstruction/Repair ○ Meniscal Root Repair Foot/Ankle |
7
8
Johnson
The DePuy Mitek HEALIX ADVANCE KNOTLESS PEEK Anchors is indicated as follows:
- . Shoulder
- Rotator Cuff Repair o
- O Bicep Tenodesis
- Deltoid Repair O
- Elbow
- Ulnar Collateral Ligament (UCL) O
- Radial Collateral Ligament (RCL) O
- Knee ●
- Posterior Oblique O
- Medial Collateral Ligament (MCL) O
- Lateral Collateral Ligament (LCL) O
- O Iliotibial (IT) Band Tenodesis
- Anterior Cruciate Ligament (ACL) Repair O
- Secondary Fixation in ACL/PCL Reconstruction/Repair O
- Meniscal Root Repair O
- Foot/Ankle ●
- Achilles Tendon Repair O
- Lateral Stabilization O
- 0 Medial Stabilization
HEALIX ADVANCE Self-Punching anchors (Note: new indications are underlined):
The DePuy Mitek HEALIX ADVANCE SP Biocomposite Anchors is indicated as follows:
- Shoulder ●
- Rotator Cuff Repair O
- Bicep Tenodesis O
- Deltoid Repair ೧
- Elbow
- Ulnar Collateral Ligament (UCL) reconstruction O
- Radial Collateral Ligament (RCL) reconstruction O
- Knee ●
- Posterior Oblique repair O
- Medial Collateral Ligament (MCL) reconstruction O
- O Lateral Collateral Ligament reconstruction
- Iliotibial (IT) Band Tenodesis O
- Anterior Cruciate Ligament (ACL) Repair o
- Secondary Fixation in ACL/PCL Reconstruction/Repair O
- Meniscal Root Repair O
The DePuy Mitek HEALIX ADVANCE SP PEEK Anchors is indicated as follows:
- Shoulder .
- 0 Rotator Cuff Repair
9
son&Johnson
| Bicep Tenodesis Deltoid Repair Elbow Ulnar Collateral Ligament (UCL) reconstruction Radial Collateral Ligament (RCL) reconstruction Knee Posterior Oblique repair Medial Collateral Ligament (MCL) reconstruction Lateral Collateral Ligament reconstruction Iliotibial (IT) Band Tenodesis Anterior Cruciate Ligament (ACL) Repair Secondary Fixation in ACL/PCL Reconstruction/Repair Meniscal Root Repair Foot/Ankle Achilles Tendon Repair Lateral Stabilization Medial Stabilization | |
|---|---|
| Non-clinical Testing | Verification activities were performed on the proposed device. Verification included an assessment of fixation strength for proposed indications at T=0 and over the healing period, as well as assessment of insertion force. |
| Safety and Performance | Results of the analyses demonstrated that the devices continue to meet established design inputs and corresponding criteria, and that there were no new issues of safety or effectiveness related to device performance. |
Based on similarities in the intended use, technological characteristics, and performance in comparison to the predicate devices, the modified HEALIX ADVANCE Knotless anchors and HEALIX ADVANCE Self-Punching anchors have shown to be substantially equivalent to the predicate devices under the Federal Food, Drug and Cosmetic Act. |