(147 days)
No
The device description and performance studies focus on the material properties and mechanical performance of a biological tissue matrix, with no mention of AI or ML.
Yes
The device is intended for the surgical repair of damaged or ruptured soft tissue membranes and reinforcement in plastic and reconstructive surgery, which are therapeutic interventions.
No
The ARTIA Tissue Matrix is a surgical mesh intended for reinforcing and repairing soft tissue, functioning as a scaffold for cellular and microvascular ingrowth. It is a reconstructive product, not a diagnostic one.
No
The device is a physical surgical mesh derived from porcine dermis, not a software program.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states it's for surgical repair and reinforcement of soft tissue. This is a therapeutic and structural application, not a diagnostic one.
- Device Description: The description details a surgical mesh derived from porcine dermis, designed to act as a scaffold for tissue ingrowth. This is consistent with a surgical implant, not a device used to examine specimens from the body.
- Lack of IVD Characteristics: There is no mention of analyzing samples (blood, urine, tissue, etc.) or providing diagnostic information about a patient's condition.
Therefore, the ARTIA Tissue Matrix is a surgical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
ARTIA Tissue Matrix is intended for use as a soft tissue patch to reinforce soft tissue where weakness exists and for the surgical repair of damaged or ruptured soft tissue membranes which require or bridging material to obtain the desired surgical outcome. The implant is intended for reinforcement in plastic and reconstructive surgery.
ARTIA Tissue Matrix is intended for single patient, one time use only.
Product codes (comma separated list FDA assigned to the subject device)
FTM, OXH
Device Description
ARTIA Reconstructive Tissue Matrix Perforated (ARTIA Tissue Matrix Perforated) is a surgical mesh that is derived from porcine dermis and is processed and preserved in a patented phosphate buffered aqueous solution containing matrix stabilizers. ARTIA Tissue Matrix Perforated is designed to perform as a surgical mesh for soft tissue repair while presenting a scaffold for cellular and microvascular ingrowth. ARTIA Tissue Matrix Perforated consists of a terminally sterilized sheet of processed porcine dermal matrix provided in various geometric configurations and packaged in a plastic holder enclosed within a pouch. The device is sterilized via electron beam irradiation. The subject device has the same underlying scientific technology, principles of operation, Intended Use and Indications for Use as the cleared predicate device, ARTIA Tissue Matrix (K142326). This 510(k) premarket notification describes a new design feature of the subject device, which introduces a 3mm diameter circular pattern of perforations (holes) throughout the tissue matrix.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
soft tissue
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)
Bench Testing: Bench testing was performed to support substantial equivalence to the predicate device. Testing and/or evaluations included relevant elements of the FDA "Guidance for the Preparation of a Premarket Notification Application for a Surgical Mesh" issued March 2, 1999. Applicable product characterization criteria used include Mesh Thickness, Tensile Strength, Device Stiffness, Suture Pull-Out Strength, Burst Strength (ASTM D6797-07(2011)), and Tear Resistance (ASTM D5735-95). Performance data demonstrates that ARTIA Tissue Matrix Perforated has similar mechanical properties and meets the established specifications as the predicate device.
Clinical Testing: No clinical testing was included in this submission.
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.
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.
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
§ 878.3300 Surgical mesh.
(a)
Identification. Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.(b)
Classification. Class II.
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Image /page/0/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal features a stylized image of three human profiles facing right, stacked on top of each other. The profiles are connected and appear to be emerging from a single base. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the image.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
February 24, 2017
Lifecell Corporation Ms. Anuja Yardi Regulatory Affairs Specialist One Millennium Way Branchburg, New Jersey 08876
Re: K162752
Trade/Device Name: ARTIA Reconstructive Tissue Matrix Perforated Regulation Number: 21 CFR 878.3300 Regulation Name: Surgical mesh Regulatory Class: Class II Product Code: FTM, OXH Dated: January 25, 2017 Received: January 26, 2017
Dear Ms. Yardi:
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 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 devicerelated 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.
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If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education 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. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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 Industry and Consumer Education 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,
David Krause -S
Binita S. Ashar, M.D., M.B.A., F.A.C.S. for Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K162752
Device Name
ARTIA Reconstructive Tissue Matrix-Perforated
Indications for Use (Describe)
ARTIA Tissue Matrix is intended for use as a soft tissue patch to reinforce soft tissue where weakness exists and for the surgical repair of damaged or ruptured soft tissue membranes which require or bridging material to obtain the desired surgical outcome. The implant is intended for reinforcement in plastic and reconstructive surgery.
ARTIA Tissue Matrix is intended for single patient, one time use only.
| 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) |
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7. 510(k) Summary
7.1 SUBMITTER
Name and Address of Submitter:
LifeCell Corporation One Millennium Way Branchburg, NJ 08876 USA
Contacts:
Anuja Yardi Regulatory Affairs Specialist Phone: (908) 947-1018 Fax: (908) 947-1095
Mira Leiwant Senior Director, Quality Engineering and Regulatory Affairs Phone: (908) 809-7747 Fax: (908) 947-1095
Prepared by and Date:
Anuja Yardi September 29, 2016
7.2 DEVICE
Name of Device: ARTIA™ Reconstructive Tissue Matrix Perforated Common or Usual Name: Surgical Mesh Classification Name: Surgical Mesh- (21 C.F.R. §878.3300) Device Class: Class II Product Code: FTM and OXH
7.3 PREDICATE DEVICE
Predicate Device:
ARTIA Reconstructive Tissue Matrix (cleared as HPTM via K142326) The predicate has not been subject to a design-related recall.
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Reference Device:
Strattice Tissue Matrix Perforated (K150712) – LifeCell Corporation The reference device has not been subject to a design-related recall.
7.4 DEVICE DESCRIPTION
ARTIA Reconstructive Tissue Matrix Perforated (ARTIA Tissue Matrix Perforated) is a surgical mesh that is derived from porcine dermis and is processed and preserved in a patented phosphate buffered aqueous solution containing matrix stabilizers. ARTIA Tissue Matrix Perforated is designed to perform as a surgical mesh for soft tissue repair while presenting a scaffold for cellular and microvascular ingrowth. ARTIA Tissue Matrix Perforated consists of a terminally sterilized sheet of processed porcine dermal matrix provided in various geometric configurations and packaged in a plastic holder enclosed within a pouch. The device is sterilized via electron beam irradiation. The subject device has the same underlying scientific technology, principles of operation, Intended Use and Indications for Use as the cleared predicate device, ARTIA Tissue Matrix (K142326). This 510(k) premarket notification describes a new design feature of the subject device, which introduces a 3mm diameter circular pattern of perforations (holes) throughout the tissue matrix.
7.5 INDICATIONS FOR USE
ARTIA Tissue Matrix is intended for use as a soft tissue patch to reinforce soft tissue where weakness exists and for the surgical repair of damaged or ruptured soft tissue membranes which require the use of reinforcing or bridging material to obtain the desired surgical outcome. The implant is intended for reinforcement in plastic and reconstructive surgery.
ARTIA Tissue Matrix is intended for single patient, one time use only.
7.6 COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICE
The subject and predicate devices are both surgical meshes derived from porcine dermis which undergo standardized, controlled manufacturing processes. Both devices consist of a terminally sterilized sheet of the processed porcine dermal matrix provided in various geometric configurations. The subject and the predicate devices share the same underlying scientific design and have the same Intended Use. Indications for Use and principles of operation and packaging configuration. Both are sterilized via electron beam irradiation.
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The subject device includes a new design feature, 3mm diameter circular pattern of perforations (holes) in the tissue matrix. The spacing and size of the perforations were evaluated against the same established performance specifications as the predicate device, ARTIA Tissue Matrix (K142326). The subject device utilizes the existing manufacturing processes of the predicate ARTIA Tissue Matrix. Perforations are added to the tissue during the final die cutting stage at the time the device is cut to its final perimeter dimensions.
7.7 PERFORMANCE
The predicate device, ARTIA Tissue Matrix (K142326) has undergone appropriate biocompatibility assessments and testing, sterilization, and viral inactivation testing. The data demonstrates that the device is biocompatible and that the manufacturing process is capable of viral inactivation. The subject device, ARTIA Tissue Matrix Perforated and the predicate device, ARTIA Tissue Matrix (K142326) utilize the same raw materials (porcine dermis), processing components/solutions, and manufacturing processes, and are identical except for the presence of perforations. The only difference in the manufacturing process of the subject device is that during the final die cutting stage, perforations will be added to the tissue at the time the device is cut to its final perimeter dimensions. The cutting dies are provided sterilized from the vendor and utilize the same base materials, and the die cutting process is the same as the predicate device. The addition of holes in the product via die cutting does not change the material properties of the tissue. Therefore, no further biocompatibility testing or viral inactivation testing was performed.
Bench Testing:
Bench testing was performed to support substantial equivalence to the predicate device. Testing and/or evaluations included relevant elements of the FDA "Guidance for the Preparation of a Premarket Notification Application for a Surgical Mesh" issued March 2, 1999. Table 1 includes the applicable product characterization criteria used to demonstrate substantial equivalence.
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| Bench Testing /Evaluation | Applicable Standard |
|---|---|
| Mesh Thickness | N/A |
| Tensile Strength | N/A |
| Device Stiffness | N/A |
| Suture Pull-Out Strength | N/A |
| Burst Strength | ASTM D6797-07(2011) |
| Tear Resistance | ASTM D5735-95 |
Performance data demonstrates that ARTIA Tissue Matrix Perforated has similar mechanical properties and meets the established specifications as the predicate device. In addition, the ARTIA Tissue Matrix Perforated Surgical Mesh shares the technological characteristics of perforations with LifeCell's other legally marketed reference device, Strattice Tissue Matrix Perforated (K150712). This new technological characteristic does not affect safety and efficacy of the device or raise new questions of safety or efficacy. ARTIA Tissue Matrix Perforated meets the requirements to perform its intended use as a soft tissue patch and is substantially equivalent to the predicate device, ARTIA Tissue Matrix (K142326).
Clinical Testing:
No clinical testing was included in this submission.
7.8 CONCLUSIONS
The subject device, ARTIA Tissue Matrix Perforated, meets the requirements to perform its intended use as a soft tissue patch and is substantially equivalent to the legally marketed predicate device, ARTIA Tissue Matrix (K142326).