Who is the manufacturer of DB-CMF?

Dimensional Bioceramics, LLC filed the 510(k) submission for DB-CMF (K182742).

What is the FDA product code for DB-CMF?

GXP. It is classified under 21 CFR 882.5300 as a Class 2 device in the Neurology panel.

What is the regulatory pathway for DB-CMF?

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

Who can help prepare an FDA 510(k) submission like DB-CMF?

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.

DB-CMF

Q: What are the predicate devices for DB-CMF?

OsteoVation® Impact (K162864).

K182742 · Dimensional Bioceramics, LLC · GXP · Jun 20, 2019 · Neurology

Device Facts

Record ID	K182742
Device Name	DB-CMF
Applicant	Dimensional Bioceramics, LLC
Product Code	GXP · Neurology
Decision Date	Jun 20, 2019
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 882.5300
Device Class	Class 2
Attributes	Therapeutic

Indications for Use

DB-Cranial is a calcium phosphate bone void filler indicated for the repair or filling of neurosurgical burr holes or other cranial bone defects and craniotomy cuts with a surface area no larger than 25 cm2. DB-Cranial may be used in the restoration or augmentation of bony contours of the cranial bone skeleton.

Device Story

DB-Cranial is a moldable, biocompatible calcium phosphate bone void filler kit; consists of alpha-tricalcium phosphate powder and sodium silicate-sodium phosphate mixing solution. Components mixed prior to implantation; applied by surgeons to repair/fill cranial defects or burr holes. Material sets in situ to form hydroxyapatite; provides structural restoration of cranial bone contours. Device is sterile, single-use; supplied in 3 cc, 5 cc, and 10 cc volumes. Benefits include stable, biocompatible material for cranial reconstruction with minimal risk of thermal necrosis during curing.

Clinical Evidence

No clinical data. Substantial equivalence demonstrated via bench testing only, including mechanical, chemical, and physical performance comparisons against the predicate device.

Technological Characteristics

Calcium phosphate bone void filler; alpha-tricalcium phosphate powder and sodium silicate-sodium phosphate liquid. Sterilized via gamma radiation (ISO 11137-2:2013, VDMax25). Sets to hydroxyapatite. Shelf life 30 months. No software or electronic components.

Indications for Use

Indicated for repair or filling of neurosurgical burr holes, cranial bone defects, and craniotomy cuts (surface area ≤ 25 cm2) and restoration/augmentation of cranial bone contours.

Regulatory Classification

Identification

Methyl methacrylate for cranioplasty (skull repair) is a self-curing acrylic that a surgeon uses to repair a skull defect in a patient. At the time of surgery, the surgeon initiates polymerization of the material and forms it into a plate or other appropriate shape to repair the defect.

Predicate Devices

OsteoVation® Impact (K162864)

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA text logo on the right. The FDA text logo is in blue and includes the letters "FDA" followed by "U.S. FOOD & DRUG ADMINISTRATION" in a smaller font size. June 20, 2019 Dimensional Bioceramics, LLC % Patsy Trisler Regulatory Consultant Trisler Consulting 5600 Wisconsin Ave. #509 Chevy Chase, Maryland 20815 Re: K182742 Trade/Device Name: DB-Cranial Regulation Number: 21 CFR 882.5300 Regulation Name: Methyl Methacrylate for Cranioplasty Regulatory Class: Class II Product Code: GXP Dated: May 20, 2019 Received: May 21, 2019 Dear Patsy Trisler: 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. 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 located at https://www.accessdata.fda.gov/scripts/cdrh/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. 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 {1}------------------------------------------------ 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 803) for devices or postmarketing safety reporting (21 CFR 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 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. 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 https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. For comprehensive regulatory information about medical devices and radiation-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, Matthew Krueger Assistant Director DHT5A: Division of Neurosurgical, Neurointerventional and Neurodiagnostic Devices OHT5: Office of Neurological and Physical Medicine Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 510(k) Number (if known) K182742 Device Name DB-Cranial Indications for Use (Describe) DB-Cranial is a calcium phosphate bone void filler indicated for the repair or filling of neurosurgical burr holes or other cranial bone defects and craniotomy cuts with a surface area no larger than 25 cm2. DB-Cranial may be used in the restoration or augmentation of bony contours of the cranial bone skeleton. | Type of Use (Select one or both, as applicable) | | |---------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------| | <div> ☑ Prescription Use (Part 21 CFR 801 Subpart D) </div> | <div> ☐ Over-The-Counter Use (21 CFR 801 Subpart C) </div> | ## CONTINUE ON A SEPARATE PAGE IF NEEDED. 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." {3}------------------------------------------------ ## 510(k) Summary DB-Cranial | I. SUBMITTER | | |----------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Submitter Name: | Dimensional Bioceramics, LLC | | Submitter Address: | 250 Natural Bridges Drive Santa Cruz, CA 95050 | | Contact Person: Telephone #: | Duran N. Yetkinler, M.D., Ph.D. 408-757-6603 | | Date Prepared: | May 6, 2019 | | II. DEVICE | | | Device Trade Name: | DB-Cranial | | Common or Usual Name: | Hydroxyapatite Cement | | Regulatory Name(s): | Methyl Methacrylate For Cranioplasty | | Classification #: | 21 CFR 882.5300 | | Product Code: | GXP | | III. PREDICATE DEVICE(s) | K162864, OsteoVation® Impact SkeletalKinetics , LLC | | IV. DEVICE DESCRIPTION | | | Device Identification, Characteristics, Sterilization and Shelf life | DB-Cranial Bone Void Filler is a moldable and biocompatible calcium phosphate bone void filler. DB-Cranial kit is comprised of two components: a calcium-phosphate powder and a mixing solution in premeasured quantities, which will be mixed together prior to implantation. | | | The 3 cc, 5 cc, and 10 cc DB-Cranial Bone Void Filler kits are provided sterile to SAL of 10-6 and are for single use only. | | | The sterilization method is gamma radiation. Sterilization validation is based on ISO 11137- 2:2013 (VDMax25). | | | DB-Cranial Bone Void Filler will be labeled with a shelf life of 30 months. | | V. INDICATIONS FOR USE | DB-Cranial is a calcium phosphate bone void filler indicated for repair or filling of neurosurgical burr holes, other cranial bone defects and craniotomy cuts with a surface area of no larger than 25cm². DB-Cranial may be used in the restoration or augmentation of bony contours of the cranial bone skeleton. | {4}------------------------------------------------ | VI. SUMMARY OF TESTING [PERFORMANCE DATA] | | | |----------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Performance Bench Testing | | | | TEST | Test Method Summary | Results | | Working Time In-Vitro | Ensures sufficient manipulation time is provided while also ensuring cement setting-times are met in the operative theater. Mixing, mold-ability, and setting strengths were measured | Both subject and predicate device reached sufficient indentation loads to ensure targeted working time and setting strength | | Setting Time | Setting tests determined strength (Mean $\geq$ 450N and $\geq$ 700N) at specified time points post sterilization and post mixing. | Subject and predicate devices achieved similar setting strengths at all time points. Strength values of these two setting cements are substantially equivalent. | | Ca to P Ratio | This test determines CA/P ratios via ICP-MS. | Both samples have a Ca/P ratio of 1.5. This test confirms both subject and predicate are composed of identical amounts of calcium and phosphate salts. | | Kit Components | Kit ingredients are compared to determine substantial equivalence. | Both subject and predicate device consist of alpha-tricalcium phosphate (Powder) and sodium silicate-sodium phosphate solution (Liquid). | | Heavy Metal Analysis | Samples are analyzed for trace heavy metal content using ICP- MS. | Trace metal limits were below allowable limits in both subject and predicate. | | pH Profile | Examines effects of the device on pH surrounding the implanted device. pH is measured in physiologic buffer solutions surrounding curing cements. | All pH readings remained within normal physiological range for both predicate and subject devices. | | FTIR Analysis | This test identifies the chemical composition of subject and predicate device following curing in simulated physiologic conditions for 24 hours then dry cured at 37°C for 72 hours. | Both subject and predicate device both show the formation of hydroxyapatite. Subject and predicate device are substantially equivalent with regards to FTIR chemical analysis. | | Crystallographic Analysis | XRD analysis is performed with samples set in simulated physiologic conditions for 2 hours, 1 day, 3 days, and 7 days. Samples are evaluated using powder x-ray diffraction and compared against known mineralogic standards. | Both subject and predicate device are confirmed identical via crystallographic analysis. The same crystalline structure over several different clinically relevant time points is formed in both materials. | | Temperature Profile | Device samples are tested in simulated physiologic solutions to measure temperature of curing cement. Temperatures above, at, and below the level of the sample are measured at 2 minute intervals over 20 minutes. | Both subject and predicate device set in an isothermic manner as designed. This demonstrates a minimal risk of thermal necrosis of tissue surrounding the implantation site. In this respect, both subject and predicate device are substantially equivalent. | | Solubility and Dissolution | Test samples are cured and incubated at simulated physiological conditions for 4 days; fluid is extracted and tested for Ca2+ concentration via ICP- AES. This experiment evaluates solubility and dissolution. | Both subject and predicate device have substantially equivalent solubility and dissolution. | | Tensile Testing | Test samples were mixed and cured for 24 hours at simulated temperature and pH. Tensile testing was performed using a mechanical tester and load at sample breakage was recorded and compared. | Subject and predicate device demonstrated identical tensile strength at 24 hours and are substantially equivalent in terms of tensile strength. | | Dimensional Stability | Dimensional stability is measured to establish that the bone void fillers maintain shape and do not dissolve in an untimely manner. | Subject and predicate are dimensionally stable materials with no discernable differences in form. | | Physical Form | Test samples were imaged by SEM to determine microstructural similarities and differences. | Both subject and predicate device demonstrated hydroxyapatite crystal formation. Subject and predicate device set to form hydroxyapatite in an identical manner. | | Biocompatibility Testing: | No biocompatibility studies were needed to demonstrate substantial equivalence. | | | Animal Testing: | No animal studies were needed to demonstrate substantial equivalence. | | | Clinical Testing: | This product type does not require clinical testing. | | | VII. COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE PREDICATE DEVICE | DB-Cranial intended use and critical specifications are substantially equivalent to the predicate device, OsteoVation Impact® (K162864), as shown by the comparative testing. There are no notable differences in comparison to the predicate device, therefore no new questions related to safety and effectiveness were raised. | | | VII. CONCLUSIONS | Based on the comparison provided and the data submitted in the 510(k), it can be concluded the DB- Cranial is substantially equivalent to the predicate device, OsteoVation Impact® (K162864). | | {5}------------------------------------------------ {6}------------------------------------------------

DB-CMF

Device Facts

Indications for Use

Device Story

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Predicate Devices

Submission Summary (Full Text)

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