(113 days)
Not Found
No
The 510(k) summary describes a physical collagen membrane for dental procedures and does not mention any software, algorithms, or AI/ML capabilities. The performance studies focus on material properties and biological response.
Yes
The device is intended for various oral surgical procedures to aid in tissue regeneration and augmentation, which are therapeutic interventions.
No
Explanation: The Collagen Dental Membrane - Conformable PP is used as a resorbable membrane material in oral surgical procedures for guided bone and tissue regeneration, acting as a structural component rather than identifying or characterizing diseases or conditions.
No
The device description clearly states it is a physical membrane made from purified porcine peritoneum, not software.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for use in "oral surgical procedures" as a "resorbable membrane material" for various bone and tissue regeneration applications. This involves direct interaction with the patient's body during surgery.
- Device Description: The description details a physical membrane made from purified porcine peritoneum, designed to be implanted.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens derived from the human body (like blood, urine, tissue samples) to provide information for diagnosis, monitoring, or screening. The device itself is the therapeutic/regenerative material being implanted.
IVD devices are used outside the body to analyze samples from the body. This device is used inside the body as a surgical implant.
N/A
Intended Use / Indications for Use
Collagen Dental Membrane - Conformable PP is intended for use in oral surgical procedures as a resorbable membrane material for use in:
- Simultaneous use of GBR-membrane and implants
- Augmentation around implants placed in immediate extraction sockets
- Augmentation around implants in delayed extraction sockets
- Localized ridge augmentation for later implantation
- Alveolar ridge reconstruction for prosthetic treatment
- Filling of bone defects after root resection, cystectomy or removal of retained teeth
- Guided bone regeneration in dehiscence defects and
- Guided tissue regeneration procedures in periodontal defects.
Product codes
NPL
Device Description
Collagen Dental Membrane - Conformable PP is a white, nonfriable, resorbable, single layered, conformable collagen membrane matrix manufactured from purified porcine peritoneum. Collagen Dental Membrane - Conformable PP is sterilized by gamma irradiation and is supplied sterile, non-pyrogenic and for single use only.
The collagen dental membrane has a thickness of approximately 0.1 to 0.8 mm and is available in the following sizes 12 x 25 mm. 15 x 20 mm, 25 x 25 mm, 20 x 30 mm, and 30 x 40 mm.
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
oral
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
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Summary of Performance Studies
Nonclinical Tests:
In vitro product characterization testing was performed to demonstrate substantial equivalence of the subject device to its predicate devices. A series of bench tests were conducted which included an evaluation of physical properties such as membrane thickness, conformability, suture strength, and an evaluation of physicochemical properties such as product permeability and hydrothermal transition temperature.
A series of in vitro and in vivo biocompatibility testing was performed to assess safety of the Collagen Dental Membrane-Conformable PP as an implantable material. The device passed all applicable FDA Blue Book Memorandum G95-1and ISO 10993-1 testing for the biological evaluation of medical devices.
Biocompatibility Tests:
- Cytotoxicity: Agarose Overlay, ISO 10993-5. Results: Non-cytotoxic; No evidence of causing any cell lysis or toxicity.
- Sensitization: Guinea Pig Maximization, ISO 10993-10. Results: No evidence of causing delayed dermal contact sensitization in the guinea pig. The test article was not considered a sensitizer in the guinea pig test.
- Intracutaneous Reactivity: Intracutaneous Study in Rabbits, ISO 10993-10. Results: Under the conditions of the study, there was no erythema or edema from the extract injected intracutaneously into rabbits. The test article extract met the requirements of the test since the difference between the mean score of the test extract and the corresponding control was passing.
- Acute Systemic Toxicity: Acute Systemic Toxicity in Mice, ISO 10993-11. Results: No mortality or evidence of systemic toxicity.
- Genotoxicity: Bacterial Reverse Mutation Study, ISO 10993-3. Results: Non-mutagenic to Salmonella typhimurium and to Escherichia coli strain WP2uvra.
- Mouse Lymphoma Assay, ISO 10993-3:2003. Results: None of the test article treatments induced substantial increases in the number of revertant colonies. Based on the criteria and conditions of the study protocol, the test article is considered non-mutagenic.
- Pyrogenicity: Rabbit Pyrogen study- USP . Results: Non-pyrogenic.
- Muscle Implantation: Muscle Implantation Study in Rabbits, 2 Weeks, ISO 10993-6. Results: The macroscopic reaction was not significant compared with the sponsor provided control article (bovine tendon collagen membrane) and not significant as compared to the negative control article (HDPE). Microscopically, the test article was classified as a nonirritant as compared to the sponsor provided control article and as a moderate irritant as compared to the negative control article.
- Subchronic Toxicity: Subcutaneous implantation study in rat. Results: Minimum tissue reaction up to 24 weeks of implantation and no adverse tissue reaction to the host.
In addition to the in vitro characterization tests, animal studies using a rabbit intraoral model, as well as a rat subcutaneous model were conducted to evaluate the in vivo stability and local tissue response to the subject device as compared to its predicate device (BioGide®).
Viral inactivation studies were performed to ensure the viral safety of the product.
Clinical Tests:
Given the similarities between Collagen Dental Membrane - Conformable PP and the predicate devices, it was determined that a clinical study would not be necessary to demonstrate substantial equivalence.
Key results: The results of the in vitro product characterization and biocompatibility testing, as well as the animal study show that Collagen Dental Membrane-Conformable PP is safe and substantially equivalent to the identified predicate devices.
Key Metrics
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 872.3930 Bone grafting material.
(a)
Identification. Bone grafting material is a material such as hydroxyapatite, tricalcium phosphate, polylactic and polyglycolic acids, or collagen, that is intended to fill, augment, or reconstruct periodontal or bony defects of the oral and maxillofacial region.(b)
Classification. (1) Class II (special controls) for bone grafting materials that do not contain a drug that is a therapeutic biologic. The special control is FDA's “Class II Special Controls Guidance Document: Dental Bone Grafting Material Devices.” (See § 872.1(e) for the availability of this guidance document.)(2) Class III (premarket approval) for bone grafting materials that contain a drug that is a therapeutic biologic. Bone grafting materials that contain a drug that is a therapeutic biologic, such as biological response modifiers, require premarket approval.
(c)
Date premarket approval application (PMA) or notice of product development protocol (PDP) is required. Devices described in paragraph (b)(2) of this section shall have an approved PMA or a declared completed PDP in effect before being placed in commercial distribution.
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Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized depiction of a human figure, represented by three overlapping profiles facing to the right. The profiles are rendered in a dark color, creating a sense of depth and unity. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the figure.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
November 5,2014
Collagen Matrix, Inc. Peggy Hansen Vice President. Clinical, Regulatory, Quality Assurance and Marketing 15 Thornton Road Oakland, New Jersey 07436
Re: K141909
Trade/Device Name: Collagen Dental Membrane - Conformable PP Regulation Number: 21 CFR 872.3930 Regulation Name: Bone grafting material Regulatory Class: Class II Product Code: NPL Dated: October 6, 2014 Received: October 9, 2014
Dear Ms. Hansen:
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.
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Page 2 - Ms. Hansen
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 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/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 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 yours,
Susan Runno DDS, mA
Erin I. Keith, M.S Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
K141909 510(k) Number (if known):
Device Name: Collagen Dental Membrane - Conformable PP
Indications for Use:
Collagen Dental Membrane - Conformable PP is intended for use in oral surgical procedures as a resorbable membrane material for use in:
- Simultaneous use of GBR-membrane and implants ●
- Augmentation around implants placed in immediate extraction sockets o
- Augmentation around implants in delayed extraction sockets ●
- Localized ridge augmentation for later implantation
- Alveolar ridge reconstruction for prosthetic treatment ●
- Filling of bone defects after root resection, cystectomy or removal of retained teeth
- Guided bone regeneration in dehiscence defects and ●
- Guided tissue regeneration procedures in periodontal defects. 0
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 NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
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510(k) SUMMARY
1. Applicant Information
| Applicant Name: | Collagen Matrix, Inc. |
|---|---|
| Address: | 15 Thornton Road |
| Oakland, New Jersey 07436 | |
| Telephone: | (201) 405-1477 |
| Fax: | (201) 405-1355 |
| Contact Person: | Peggy Hansen, RAC |
| VP, Clinical, Regulatory, QA, and Marketing | |
| Date Prepared: | October 6, 2014 |
2. Name of the Device
| Device Common Name: | Resorbable Collagen Membrane |
|---|---|
| Device Trade Name: | Collagen Dental Membrane – Conformable PP |
| Device Classification Name: | Barrier, animal source, intraoral |
| 872.3930 | |
| NPL | |
| Class II |
3. Legally Marketed Devices to Which Substantial Equivalence is Claimed
Predicate Device(s):
BIO-GIDE® K042197
Collagen Dental Membrane V K100156
4. Description of the Device
Collagen Dental Membrane - Conformable PP is a white, nonfriable, resorbable, single layered, conformable collagen membrane matrix manufactured from purified porcine peritoneum. Collagen Dental Membrane - Conformable PP is sterilized by gamma irradiation and is supplied sterile, non-pyrogenic and for single use only.
The collagen dental membrane has a thickness of approximately 0.1 to 0.8 mm and is available in the following sizes 12 x 25 mm. 15 x 20 mm, 25 x 25 mm, 20 x 30 mm, and 30 x 40 mm.
5. Intended Use
Collagen Dental Membrane - Conformable PP is intended for use in oral surgical procedures as a resorbable membrane material for use in:
- · Simultaneous use of GBR-membrane and implants
- · Augmentation around implants placed in immediate extraction sockets
- · Augmentation around implants in delayed extraction sockets
- · Localized ridge augmentation for later implantation
4
- · Alveolar ridge reconstruction for prosthetic treatment
- · Filling of bone defects after root resection, cystectomy or removal of retained teeth
- · Guided bone regeneration in dehiscence defects and
- · Guided tissue regeneration procedures in periodontal defects.
6. Summary/Comparison of Technical Characteristics
Collagen Dental Membrane-Conformable PP and its predicate devices have similar technological characteristics. In particular, the Collagen Dental Membrane-Conformable PP and its predicates are similar with respect to intended use, material (porcine peritoneum), form, sizes, thickness, physical integrity, permeability and conformability.
Nonclinical Tests Submitted
The substantial equivalence of Collagen Dental Membrane-Conformable PP and its predicates was demonstrated based on in vitro characterization studies, biocompatibility studies, in vivo animal studies, and clinical history of the predicate devices.
In vitro product characterization testing was performed to demonstrate substantial equivalence of the subject device to its predicate devices. A series of bench tests were conducted which included an evaluation of physical properties such as membrane thickness, conformability, suture strength, and an evaluation of physicochemical properties such as product permeability and hydrothermal transition temperature.
A series of in vitro and in vivo biocompatibility testing was performed to assess safety of the Collagen Dental Membrane-Conformable PP as an implantable material. The device passed all applicable FDA Blue Book Memorandum G95-1and ISO 10993-1 testing for the biological evaluation of medical devices.
| Test | Test Method/Model | Results |
|---|---|---|
| Cytotoxicity | Agarose Overlay, ISO | |
| 10993-5 | Non-cytotoxic; No evidence of causing any cell | |
| lysis or toxicity. | ||
| Sensitization | Guinea Pig | |
| Maximization, ISO | ||
| 10993-10 | No evidence of causing delayed dermal contact | |
| sensitization in the guinea pig. The test article | ||
| was not considered a sensitizer in the guinea pig | ||
| test. | ||
| Intracutaneous | ||
| Reactivity | Intracutaneous Study in | |
| Rabbits, ISO 10993-10 | Under the conditions of the study, there was no | |
| erythema or edema from the extract injected | ||
| intracutaneously into rabbits. The test article | ||
| extract met the requirements of the test since the | ||
| difference between the mean score of the test | ||
| extract and the corresponding control was | ||
| passing. | ||
| Acute Systemic | ||
| Toxicity | Acute Systemic Toxicity | |
| in Mice, ISO 10993-11 | No mortality or evidence of systemic toxicity. | |
| Genotoxicity | Bacterial Reverse | |
| Mutation Study, ISO | ||
| 10993-3 | Non-mutagenic to Salmonella typhimurium and | |
| to Escherichia coli strain WP2uvra. |
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| Test | Test Method/Model | Results |
|---|---|---|
| Mouse Lymphoma | ||
| Assay, ISO 10993- | ||
| 3:2003 | None of the test article treatments induced | |
| substantial increases in the number of revertant | ||
| colonies. Based on the criteria and conditions of | ||
| the study protocol, the test article is considered | ||
| non-mutagenic. | ||
| Pyrogenicity | Rabbit Pyrogen study- | |
| USP | Non-pyrogenic | |
| Muscle | ||
| Implantation | Muscle Implantation | |
| Study in Rabbits, 2 | ||
| Weeks, ISO 10993-6 | The macroscopic reaction was not significant | |
| compared with the sponsor provided control | ||
| article (bovine tendon collagen membrane) and | ||
| not significant as compared to the negative | ||
| control article (HDPE). Microscopically, the test | ||
| article was classified as a nonirritant as | ||
| compared to the sponsor provided control article | ||
| and as a moderate irritant as compared to the | ||
| negative control article. | ||
| Subchronic | ||
| Toxicity | Subcutaneous | |
| implantation study in rat. | Minimum tissue reaction up to 24 weeks of | |
| implantation and no adverse tissue reaction to | ||
| the host. |
In addition to the in vitro characterization tests, animal studies using a rabbit intraoral model, as well as a rat subcutaneous model were conducted to evaluate the in vivo stability and local tissue response to the subject device as compared to its predicate device (BioGide®).
Viral inactivation studies were performed to ensure the viral safety of the product.
Clinical Test Submitted
Given the similarities between Collagen Dental Membrane - Conformable PP and the predicate devices, it was determined that a clinical study would not be necessary to demonstrate substantial equivalence.
7. Conclusion of Non-clinical Studies
The results of the in vitro product characterization and biocompatibility testing, as well as the animal study show that Collagen Dental Membrane-Conformable PP is safe and substantially equivalent to the identified predicate devices.