← Product Code [GWO](/submissions/NE/subpart-f%E2%80%94neurological-therapeutic-devices/GWO) · K112812 # LEFORTE NEURO SYSTEM BONE PLATE (K112812) _Jeil Medical Corporation · GWO · Feb 22, 2012 · Neurology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/NE/subpart-f%E2%80%94neurological-therapeutic-devices/GWO/K112812 ## Device Facts - **Applicant:** Jeil Medical Corporation - **Product Code:** [GWO](/submissions/NE/subpart-f%E2%80%94neurological-therapeutic-devices/GWO.md) - **Decision Date:** Feb 22, 2012 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 882.5320 - **Device Class:** Class 2 - **Review Panel:** Neurology - **Attributes:** Therapeutic ## Indications for Use This device is intended for use in selective trauma of the cranial skeleton, cranial surgery and reconstructive procedures. ## Device Story LeForte Neuro System Bone Plate & Screw consists of titanium plates and screws used for rigid fixation in cranial surgery, trauma, and reconstruction. Device provides mechanical stabilization of bone segments. Operated by surgeons in clinical/surgical settings. Output is physical fixation of bone; aids healing by maintaining alignment. Benefits include structural support for cranial bone during recovery. Device is non-sterile, single-use, and requires surgical implantation. ## Clinical Evidence No clinical data. Bench testing only. ## Technological Characteristics Materials: Pure Titanium (ASTM F67) for plates, Titanium Alloy (ASTM F136) for screws. Plate thickness 0.3-0.6mm; screw diameter 1.4-1.9mm; screw length 2.2-5.0mm. Surface treatment: Anodizing on plates. Non-sterile, single-use. Mechanical fixation device. ## Regulatory Identification A preformed alterable cranioplasty plate is a device that is implanted into a patient to repair a skull defect. It is constructed of a material, e.g., tantalum, that can be altered or reshaped at the time of surgery without changing the chemical behavior of the material. ## Predicate Devices - LeForte Neuro System Bone Plate ([K091679](/device/K091679.md)) - LeForte Neuro System Bone Plate ([K103778](/device/K103778.md)) - LeForte Neuro System Bone Screw ([K091686](/device/K091686.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K112812 FEB 2 2 2012 ## 510 (k) Summary This summary of 510(k) safety and effectiveness information is being submitted in accordance with requirements of 21 CFR Part 807.92 Date: January 17, 2012 #### 1. Contact: | | Company | |----------|-------------------------------------------------------------------------------------------------| | Name | Jeil Medical Corporation | | Address | #702, Kolon Science Valley 2nd
811, Guro-dong, Guro-gu, Seoul, 152-050,
Republic of Korea | | Phone | +82 2 850-3524 | | Fax | +82 2 850-3525 | | Contact | Mr. Ron Arkin | | Internet | ronarkin@arkinconsulting.com | #### 2. Device: | · Proprietary Name - | LeForte Neuro System Bone Plate & Screw | |-------------------------|-------------------------------------------| | · Common Name - | Bone Plate, Bone Screw | | · Classification Name - | Plate, Cranioplasty, Preformed, Alterable | Plate, Cranioplasty, Preformed, Alterable Fastener, Plate, Cranioplasty #### 3. Predicate Devices: . - Jeil Medical Corporation/ LeForte Neuro System Bone Plate / K091679 . - Jeil Medical Corporation/ LeForte Neuro System Bone Plate / K103778 . - Jeil Medical Corporation/ LeForte Neuro System Bone Screw / K091686 - 4. Regulatory Classifications, Product Code: 21CFR882.5320, GWO, Class II 21CFR882.5360, HBW, Class II #### 5. Performance Standards: No applicable performance standards have been issued under section 514 or under section 513(b) of the Food, Drug and Cosmetic Act. - 6. Description: The LeForte Neuro System Bone Plate & Screw is made of pure Titanium (ASTM F67) and Titanium Alloy (ASTM F136). It is intended for use in selective trauma of the cranial skeleton, cranial surgery and reconstructive procedures. {1}------------------------------------------------ LeForte Neuro System Bone Plate & Screw - 7. Indications for Use: This device is intended for use in selective trauma of the cranial skeleton, cranial surgery and reconstructive procedures. - 8. Contraindications: - · Not for use in cases of active or suspected infection or in patients previously sensitized to Titanium. - · Not for use in patients exhibiting disorders which would cause the patient to ignore the limitations of rigid fixation plate and screw implants. - 9. Potential Adverse Affects: - Poor bone formulation, Osteoporosis, Osteolysis, Osteomyelitis, inhibited revascularization, or infection can cause loosening, bending, cracking or fracture of the device or premature loss of fixation with the bone, leading to nonunion, - Nonunion or delayed union which may lead to breakage of the implant - Migration, bending, fracture or loosening of the implant - Metal sensitivity, or allergic reaction to foreign body " - . Decrease in bone density due to stress shielding - . Pain, discomfort, or abnormal sensation due to the presence of the device - . Increased fibrous tissue response around the fracture site and/or the implant - . Necrosis of bone - . Inadequate healing Apart from these adverse effects there are always possible complications of any surgical procedure such as but not limited to, infection, nerve damage and pain which may not be related to the implant. - 10. Predicate comparison: The LeForte Neuro System Bone Plate & Screw has the same device characteristics, material, design and intended use as the predicate devices identified. | Parameter | LeForte Neuro System
Bone Plate & Screw
Jeil Medical Corporation | LeForte Neuro System Bone Plate,
LeForte Neuro System Bone Screw
Jeil Medical Corporation | |------------------------|--------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | K# | Modified
v | K091679, K103778, K091686 | | Indications
for use | This device is intended for use in selective trauma of the cranial skeleton,
cranial surgery and reconstructive procedures. | | | Shape | The same models with the addition of
Triangular shapes | Mesh, Straight, Y, Curved, Square,
Quad, X, Calvarium, Double Y, Gap,
Bur hole, Mesh_MA, Mesh_MB,
Mesh_MC, Mesh_MD, NF Auto
Screw-Micro, NF Auto Screw-Mid | | Dimensional | Plate thickness 0.3~0.6m
Screw Outer diameter 1.4~1.9mm
Screw Length 2.2~5.0mm | Plate thickness 0.3~0.6m
Screw Outer diameter 1.4~1.9mm
Screw Length 3.0~5.0mm | | Material | Plate - Titanium ASTM F67 Grade1, 2, 3
Screw - Titanium Alloy ASTM F136 | | {2}------------------------------------------------ #### LeForte Neuro System Bone Plate & Screw | Parameter | LeForte Neuro System
Bone Plate & Screw
Jeil Medical Corporation | LeForte Neuro System Bone Plate,
LeForte Neuro System Bone Screw
Jeil Medical Corporation | |---------------|------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------| | Surface | Plate: Anodizing
Screw: N/A | | | Sterilization | Non sterile | | | Single use | Yes | | | Packaging | Vial, PA+PE film sealing | | ## l 1. Conclusions: : : . : In accordance with the Federal Food, Drug and Cosmetic Act, 21 CFR Part 807, and based on the information provided in this premarket notification Jeil Medical Corporation Concludes that the LeForte Neuro System Bone Plate & Screw is safe and effective and substantially equivalent to the predicate device as described herein. {3}------------------------------------------------ ## DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image is a black and white circular seal for the Department of Health & Human Services USA. The seal features the department's logo, which is an abstract image of an eagle. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged around the perimeter of the circle. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002 Jeil Medical Corporation c/o Mr. Paul Sumner Official Correspondent Arkin Consulting Group LLC 1733 Canton Lane Marietta, GA 30062 Re: K112812 LeForte Neuro System Bone Plate & Screw Regulation Number: 21 CFR 882.5320 Regulation Name: Preformed alterable cranioplasty plate Regulatory Class: Class II Product Code: GWO, GXR, HBW Dated: January 19, 2012 Received: January 23, 2012 Dear Mr. Sumner: 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 FEB 2 2 2012 {4}------------------------------------------------ Page 2 - Mr. Paul Sumner device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) 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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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 Small Manufacturers. International and Consumer Assistance 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, Kesia Alexander Malvina B. Eydelman, M.D. Director Division of Ophthalmic, Neurological, and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ LeForte Neuro System Bone Plate & Screw # Indications for Use Statement 510(k) K112812 Number (if known) Device LeForte Neuro System Bone Plate & Screw Name This device is intended for use in selective trauma of the cranial skeleton, Indications for Use cranial surgery and reconstructive procedures. Prescription Use (Per 21 CFR 801. Subpart D) OR Over-The-Counter Use (21CFR801 Subpart C) ### PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED Concurrence of CDRH, Office of Device Evaluation (ODE) Lia Nguyen **(Division Sign-Off)** Division of Ophthalmic, Neurological and Ear, Nose and Throat Devices K 11-2812 510(k) Number_ Indications For Use Statement --- **Source:** [https://fda.innolitics.com/submissions/NE/subpart-f%E2%80%94neurological-therapeutic-devices/GWO/K112812](https://fda.innolitics.com/submissions/NE/subpart-f%E2%80%94neurological-therapeutic-devices/GWO/K112812) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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