Who is the manufacturer of DIAPHRAGMATIC HERNIA GRAFT?

Cook Biotech, Inc. filed the 510(k) submission for DIAPHRAGMATIC HERNIA GRAFT (K133011).

What is the FDA product code for DIAPHRAGMATIC HERNIA GRAFT?

OWV. It is classified under 21 CFR 878.3300 as a Class 2 device in the General, Plastic Surgery panel.

What is the regulatory pathway for DIAPHRAGMATIC HERNIA GRAFT?

510(k) clearance (submission type: Traditional).

What are the predicate devices for DIAPHRAGMATIC HERNIA GRAFT?

SIS Hernia Repair Device (K974540/K062697); Surgisis Staple Line Reinforcement (K022044); Permacol™ Surgical Implant (K120605).

Who can help prepare an FDA 510(k) submission like DIAPHRAGMATIC HERNIA GRAFT?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

DIAPHRAGMATIC HERNIA GRAFT

K133011 · Cook Biotech, Inc. · OWV · Jun 20, 2014 · General, Plastic Surgery

Device Facts

Record ID	K133011
Device Name	DIAPHRAGMATIC HERNIA GRAFT
Applicant	Cook Biotech, Inc.
Product Code	OWV · General, Plastic Surgery
Decision Date	Jun 20, 2014
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 878.3300
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The Diaphragmatic Hernia Graft is intended for implantation to reinforce soft tissues where weakness exists, including the repair of diaphragmatic/hiatal hernias. The graft is supplied sterile and intended for one time use.

Device Story

Diaphragmatic Hernia Graft is a sterile, single-use surgical mesh composed of multiple layers of bioabsorbable porcine small intestinal submucosa (SIS) collagen matrix. The graft is supplied in a dried state within a sealed double pouch. It is intended for implantation by surgeons to reinforce soft tissues and repair diaphragmatic/hiatal hernias. The device features resorbable stitching to improve handling and reduce delamination during implantation. By providing a scaffold for tissue reinforcement, the graft supports the repair of hernias and body wall defects. Clinical benefit is derived from the biocompatible nature of the SIS material, which integrates into the body to provide mechanical strength for the repair site.

Clinical Evidence

Evidence includes biocompatibility testing (ISO 10993-1), mechanical bench testing, animal studies for diaphragmatic/hiatal hernia repair, and clinical study data for the base SIS material. Clinical outcomes confirm the safety and biocompatibility of the SIS material in hernia repair applications. Performance of the specific rectangular and U-shape configurations was validated as adequate in patients.

Technological Characteristics

Material: Porcine small intestinal submucosa (SIS) collagen (Types I, III, IV, VI). Dimensions: 7 x 10 cm (rectangular or U-shape). Thickness: 0.1 - 1.5 mm. Features: Resorbable stitching for handling/delamination resistance. Sterilization: Sterile. Biocompatibility: ISO 10993-1 compliant.

Indications for Use

Indicated for patients requiring soft tissue reinforcement, specifically for the repair of diaphragmatic or hiatal hernias.

Regulatory Classification

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.

Predicate Devices

SIS Hernia Repair Device (K974540/K062697)
Surgisis Staple Line Reinforcement (K022044)
Permacol™ Surgical Implant (K120605)

Related Devices

K133306 — SIS HERNIA GRAFT · Cook Biotech, Inc. · Jul 23, 2014
K171817 — Biodesign Diaphragmatic Hernia Graft · Cook Biotech Incorporated · Mar 13, 2018
K111695 — HYBRID GRAFT · Cook Biotech, Inc. · Apr 2, 2012
K062697 — SIS HERNIA REPAIR DEVICE, SURGISIS GOLD HERNIA REPAIR GRAFT · Cook Biotech, Inc. · Oct 13, 2006
K162934 — Biodesign Parastomal Hernia Repair Graft · Cook Biotech Incorporated · Jul 10, 2017

Submission Summary (Full Text)

{0}------------------------------------------------ # 510(k) Summary # June 19, 2014 # JUN 2 0 2014 # Cook Biotech Incorporated #### Diaphragmatic Hernia Graft Manufacturer Name: Cook Biotech Incorporated 1425 Innovation Place West Lafayette, Indiana 47906 Telephone: +1 (765) 497-3355 FAX: +1 (765) 807-7709 Official Contact: Perry W. Guinn #### DEVICE NAME AND CLASSIFICATION | Trade/Proprietary Name: | Diaphragmatic Hernia Graft | |-----------------------------|----------------------------------| | Common Name: | Surgical mesh | | Classification Regulations: | Class II, 21 CFR §878.3300 (FTM) | #### INTENDED USE: The Diaphragmatic Hernia Graft is intended for implantation to reinforce soft tissues where weakness exists, including the repair of diaphragmatic/hiatal hernias. The graft is supplied sterile and intended for one time use. #### DEVICE DESCRIPTION: The Diaphragmatic Hernia Graft is composed of multiple layers of a bioabsorbable, extracellular collagen membrane matrix (Small Intestinal Submucosa, SIS) that are held together with a biodegradable suture to improve the device handling characteristics at the time of implant. The Diaphragmatic Hernia Graft is identical in its base material to its predicates SIS Hernia Repair Device (K974540/K062697) and Surgisis Staple Line Reinforcement (K022044), also manufactured by Cook Biotech Incorporated, and similar to its predicate Permacol™ Surgical Implant (K120605), manufactured by Covidien. The Diaphragmatic Hernia Graft is substantially equivalent to its SIS predicates in that its technology is able to be incorporated into the body. The device is also substantially equivalent to its predicates in its intended use for reinforcement and repair of diaphragmatic/hiatal hernias. The device is packaged in a dried state and supplied sterile in a sealed double pouch system. {1}------------------------------------------------ # EQUIVALENCE TO MARKETED DEVICES The Diaphragmatic Hernia Graft is substantially equivalent to its predicate devices with respect to intended use, materials and technological characteristics, in terms of section 510(k) substantial equivalence, as shown in biocompatibility testing (conducted in accordance to ISO 10993-1 standards), mechanical, pre-clinical and clinical testing. #### Biocompatibility Testing The following biocompatibility tests were performed on sterilized SIS devices, which are identical in base material to the Diaphragmatic Hernia Graft (according to the ISO 10993-1 standard): - Genotoxicity . - Direct contact in vitro hemolysis . - Cytotoxicity � - . Muscle implantation - Acute intracutaneous reactivity - Skin irritation . - . ISO Sensitization - Acute systemic toxicity ● - Pyrogenicity ● - . LAL endotoxins - Subchronic systemic toxicity ● The results of these tests provided evidence that the Diaphragmatic Hernia Graft meets biocompatibility requirements of the ISO standard. #### Mechanical Testing The Diaphragmatic Hernia Graft material was tested for the following: - Suture retention strength . - . Burst strength - Tensile strength � - Stiffness . The results of the mechanical testing provide evidence that the Diaphragmatic Hernia Graft possesses adequate mechanical strength for its application. {2}------------------------------------------------ ### Animal Testing The SIS material that comprises the Diaphragmatic Hernia Graft has been tested in animal studies for diaphragmatic/hiatal hernia repair. These animal studies provide evidence that the Diaphragmatic Hernia Graft is biocompatible and safe in its application. # Clinical Testing The performance of Surgisis (which is made of SIS, the same base material as the Diaphragmatic Hernia Graft) was assessed in several different clinical studies. The clinical outcomes of these studies show that the SIS material, which comprises the Diaphragmatic Hernia Graft, is safe and biocompatible. Further clinical evidence was submitted showing that the rectangular flat sheet and U-shape configurations of the Diaphragmatic Hernia Graft performed adequately in patients. These studies provide evidence that the Diaphragmatic Hernia Graft is substantially equivalent to its predicates in this application. # Substantial Equivalence See Table 1 for a comparison of the subject device and its predicates. | Device | Diaphragmatic Hernia Graft | SIS Hernia Repair Device | Surgisis Staple Line Reinforcement | Permacol Surgical Implant | |---------------|----------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Manufacturer | Cook Biotech Incorporated | Cook Biotech Incorporated | Cook Biotech Incorporated | Covidien | | 510(k) Number | K133011 | K974540/K062697 | K022044 | K120605 | | Intended Use | For implantation to reinforce soft tissues where weakness exists, including the repair of diaphragmatic/hiatal hernias. | To be implanted to reinforce soft tissues where weakness exists. Indications for use include the repair of a hernia or body wall defect. | For use as a prosthesis for the surgical repair of soft tissue deficiencies using surgical staplers. The device may be used for buttressing and reinforcing staple lines during lung resection (e.g., wedge resection, blebectomy, lobectomy, bullectomy, bronchial resection, segmenteectomy, pneumonectomy/pneumect omy, pneumoreduction) and other incisions and excisions of the lung and bronchus. The device can be used for the reinforcement of the gastric staple line during the bariatric surgical | Intended for use as a soft tissue implant to reinforce soft tissue where weakness exists and for the surgical repair of damaged or ruptured soft tissue membranes. It is specifically indicated for the repair of abdominal, inguinal, diaphragmatic, femoral, scrotal, umbilical, incisional, parastomal hernias and abdominal wall defects. | # Table 1 - Substantial Equivalence Comparison {3}------------------------------------------------ | Device | Diaphragmatic Hernia Graft | SIS Hernia Repair Device | Surgisis Staple Line Reinforcement | Permacol Surgical Implant | |------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------| | | | | bypass and gastric banding. The device can also be used for abdominal and thoracic wall repair, muscle flap reinforcement, trans- abdominal rectal and vaginal prolapse repair, trans-abdominal reconstruction of the pelvic floor, and repair of hernias (e.g., diaphragmatic, femoral, incisional, inguinal, lumbar, paracolostomy, scrotal, umbilical). The Surgisis Staple Line Reinforcement may be used with anastomotic staplers or with non-anastomotic staplers. | | | Material | Porcine small intestinal submucosa (porcine) Primarily Types I, III, IV and VI collagen (constituents of the extracellular matrix) | Porcine small intestinal submucosa (porcine) Primarily Types I, III, IV and VI collagen (constituents of the extracellular matrix) | Porcine small intestinal submucosa (porcine) Primarily Types I, III, IV and VI collagen (constituents of the extracellular matrix) | Porcine dermis (collagen) | | Dimensions | Nominally, 7 x 10 cm (a rectangular flat sheet configuration and a U shaped configuration). The rectangular sheet has resorbable stitching across the graft and the U-shape graft is stitched on the edges to reduce delamination during implantation | 5 x 8 cm to 20 x 30 cm | 1.0 x 3.8 cm to 1.2 x 8.8 cm | 1 cm x 4 cm to 28cm x 40 cm | | Thickness | 0.1 - 1.5 mm | 0.1 - 1.5 mm | 0.350 mm | 0.5-1.5 mm | ・、・・・・ CONCLUSION: The biocompatibility, mechanical, pre-clinical and clinical tests performed on the Diaphragmatic Hernia Graft show that the device is substantially equivalent to its predicates. . {4}------------------------------------------------ DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/4/Picture/1 description: The image shows the words "Public Health Service" in a bold, sans-serif font. The text is arranged on a single line, with each word clearly legible. The overall impression is that of an official or formal heading. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 June 20, 2014 Cook Biotech Incorporated Mr. Perry W. Guinn, Vice President Regulatory Affairs and Quality Assurance 1425 Innovation Place West Lafayette, Indiana 47906 Re: K133011 Trade/Device Name: Diaphragmatic Hernia Graft Regulation Number: 21 CFR 878.3300 Regulation Name: Surgical mesh Regulatory Class: Class II Product Code: OWV, FTM Dated: May 20, 2014 Received: May 21, 2014 Dear Mr. Guinn: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviews 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 that I DI Hos Intellites and regulations administered by other Federal agencies. You must or any I vith 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 {5}------------------------------------------------ Page 2 - Mr. Perry W. Guinn 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 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" (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 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/Resourcesfor You/Industry/default.htm. Sincerely yours. # David Kranse -S for Binita S. Ashar, M.D., M.B.A., F.A.C.S. Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ #### DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration # Indications for Use 510(k) Number (if known) K133011 Device Name Diaphragmatic Hernia Graft #### Indications for Use (Describe) The Diaphragmatic Hernia Graft is intended for implantation to reinforce soft tissue where weakness exists, including the repair of diaphragmatic/hiatal hernias. The graft is supplied sterile and intended for one time use. 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) # PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED. FOR FDA USE ONLY Concurrence of Center for Devices and Radiological Health (CDRH) (Signature) Peter L. Hudson -S 2014.06.20 13:12:26 -04'00' This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW." The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement below.