(267 days)
No
The device description focuses on the physical components (plates, screws) and their material properties and mechanical performance. There is no mention of software, algorithms, or data processing that would indicate the use of AI/ML.
No
The device is described as a cranial plating system intended for internal fixation of fractures, osteotomies, and reconstruction of bony defects. These are structural repairs, not therapeutic treatments for disease or dysfunctional conditions.
No
The device is described as a cranial plating system for internal fixation and reconstruction of the cranial skeleton, not for diagnosing conditions.
No
The device description clearly states it consists of bone screws, mating bone plates, and panels, which are physical hardware components made of titanium.
Based on the provided text, the NeuroPro® Low Profile Cranial Plating System is not an IVD (In Vitro Diagnostic) device.
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or screening.
- NeuroPro® System Function: The description clearly states that the NeuroPro® system is used for the internal fixation, reconstruction, and stabilization of the cranial skeleton. This is a surgical implant used directly on the patient's bone, not for testing samples outside the body.
- Intended Use: The intended use focuses on surgical procedures related to cranial bone.
- Device Description: The description details the physical components (plates, screws) and their materials, all of which are consistent with a surgical implant.
Therefore, the NeuroPro® Low Profile Cranial Plating System is a surgical device, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The NeuroPro® Low Profile Cranial Plating System Family is intended for internal fixation of fractures and osteotomies of the cranial skeleton, internal fixation of cranial bone flap osteotomies and reconstruction of bony defects and deficits in the cranial skeleton.
The NeuroPro® Low Profile Cranial Plating System is not indicated for use in the spine or high load bearing applications.
Product codes
GWO, GXR, HBW
Device Description
The NeuroPro® Low Profile Cranial Plating System provides rigid fixation of cranial bone flaps with a thin profile for reduced palpability. The system consists of bone screws and mating bone plates and panels with a beveled plate edge and thinner profile to reduce palpability. Malleable bone plates and panels are easily shaped by hand and/or with stainless steel instruments. The bone screws are used to secure various shapes of bone plates and panels to the cranium. The NeuroPro® Low Profile plates and panels are manufactured from Commercially Pure Titanium and meet all of the specifications of ISO 5832-2 or ASTM F-67. The NeuroPro® Low Profile screws are manufactured from 6AV4V ELI (Extra Low Interstitial) Titanium Allov and meet all of the specifications of ISO 5832-3 or ASTM F-136.
The NeuroPro® Low Profile Cranial Plating System is a modification of the standard NeuroPro® Cranial Plating System to be made thinner than those in the original submission (K964362), with exception of the hex panels which are the same thickness.
The NeuroPro® Low Profile Cranial Plating Screws are a modification of the standard NeuroPro® Quick Tap® Bone Screws to have a shorter screw head height than those in the original submission (K982927). The plates, panels and screws are similar in sizes, dimensions and identical in functionality as the standard NeuroPro® Cranial Plating System which was cleared as part of the original 510(k) submission (K964362).
The NeuroPro® Low Profile Cranial Plating System is identical to the standard NeuroPro® Cranial Plating System in terms of intended use, indications for use, material of construction, manufacturing process, functionality, compatibility of the plates and panels with all screw types, shelf life, biocompatibility, packaging and sterilization method.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Cranial skeleton
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
Performance testing of the NeuroPro® Low Profile Cranial Plating System was conducted in accordance with various international standards and internal Kinamed methods. All of the NeuroPro® Low Profile components are made of materials which conform to international and/or FDA recognized consensus standards for the type of material. All of these materials have a long successful history in similar neurosurgical implant applications. The NeuroPro® Low Profile Cranial Plating System was tested as part of design verification/validation to Kinamed test methods with pre-defined acceptance criteria. As applicable, the testing was conducted on the worst case component size and option/design. Bone plates and panels were subjected to bend testing according to ASTM F67-06. Bone screw testing consisted of the following Kinamed test methods: Rate of Insertion (Amount of screw advancement per revolution), Ease of Insertion (Driving torque required per revolution), Torsional Strength, Screwdriver Interface Integrity, Simulated Use in Animal Bone. The testing met all acceptance criteria and verifies that the performance of the NeuroPro® Low Profile Cranial Plating System is substantially equivalent to the predicate devices.
Key Metrics
Not Found
Predicate Device(s)
K964362 NeuroPro® Cranial Plating System, K982927 NeuroPro® Quick Tap® Bone Screws, K911936 OsteoMed® Fast-Flap ™ Neuro Fixation System, K953385 Biomet® ThinFlap™ Lorenz® Plating System Neuro, K974785 OsteoMed® Auto-Drive Bone Screw
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 882.5320 Preformed alterable cranioplasty plate.
(a)
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.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/1 description: The image shows the logo for KINAMED Incorporated. The logo features a stylized letter K on the left side. To the right of the K is the word "KINAMED" in bold, uppercase letters, with a small dot after the D. Below "KINAMED" is the word "INCORPORATED" in smaller, uppercase letters.
Traditional 510(k) Summary
APR 0 5 2013
| Manufacturer: | KINAMED® Incorporated
820 Flynn Road
Camarillo, CA 93012-8701
USA |
|-----------------|--------------------------------------------------------------------------------------|
| | Phone (805) 384-2748
FAX (805) 384-2792 |
| Contact Person: | Heather Neely, RAC
Senior Director of Quality Assurance and Regulatory Compliance |
Kinamed®, Inc. Phone (805) 384-2748 x210 FAX (805) 384-2792 email: hneely@kinamed.com
Date Prepared: July 11, 2012, revised February 15, 2013
DEVICE INFORMATION
| Trade/Proprietary Name: | NeuroPro® Low Profile Cranial Plating System 510(k) |
|---|---|
| Common Name: | |
| Classification Name: | Cranial Plating System |
| Preformed alterable cranioplasty plate, 21 CFR | |
| 882.5320 | |
| Burr Hole Cover, 21 CFR 882.5250 | |
| Cranioplasty plate fastener, 21 CFR 882.5360 | |
| Class II | |
| Device Product Code: GWO, Preformed alterable | |
| cranioplasty plate | |
| GXR, Burr Hole Cover | |
| HBW, Cranioplasty plate | |
| fastener | |
| Predicate Devices: | K964362 NeuroPro® Cranial Plating System |
| K982927 NeuroPro® Quick Tap® Bone Screws | |
| K911936 OsteoMed® Fast-Flap ™ Neuro Fixation System | |
| K953385 Biomet® ThinFlap™ Lorenz® Plating System Neuro | |
| K974785 OsteoMed® Auto-Drive Bone Screw | |
| NeuroPro® Low Profile Cranial Plating System 510(k) | |
| February 15, 2013 | Section 5 Additional Information - Page 2 of 5 |
1
Product Description:
The NeuroPro® Low Profile Cranial Plating System provides rigid fixation of cranial bone flaps with a thin profile for reduced palpability. The system consists of bone screws and mating bone plates and panels with a beveled plate edge and thinner profile to reduce palpability. Malleable bone plates and panels are easily shaped by hand and/or with stainless steel instruments. The bone screws are used to secure various shapes of bone plates and panels to the cranium. The NeuroPro® Low Profile plates and panels are manufactured from Commercially Pure Titanium and meet all of the specifications of ISO 5832-2 or ASTM F-67. The NeuroPro® Low Profile screws are manufactured from 6AV4V ELI (Extra Low Interstitial) Titanium Allov and meet all of the specifications of ISO 5832-3 or ASTM F-136.
The NeuroPro® Low Profile Cranial Plating System is a modification of the standard NeuroPro® Cranial Plating System to be made thinner than those in the original submission (K964362), with exception of the hex panels which are the same thickness.
The NeuroPro® Low Profile Cranial Plating Screws are a modification of the standard NeuroPro® Quick Tap® Bone Screws to have a shorter screw head height than those in the original submission (K982927). The plates, panels and screws are similar in sizes, dimensions and identical in functionality as the standard NeuroPro® Cranial Plating System which was cleared as part of the original 510(k) submission (K964362).
The NeuroPro® Low Profile Cranial Plating System is identical to the standard NeuroPro® Cranial Plating System in terms of intended use, indications for use, material of construction, manufacturing process, functionality, compatibility of the plates and panels with all screw types, shelf life, biocompatibility, packaging and sterilization method.
Indications for Use:
The NeuroPro® Low Profile Cranial Plating System Family is intended for internal fixation of fractures and osteotomies of the cranial skeleton, internal fixation of cranial bone flap osteotomies and reconstruction of bony defects and deficits in the cranial skeleton.
The NeuroPro® Low Profile Cranial Plating System is not indicated for use in the spine or high load bearing applications.
NeuroPro® Low Profile Cranial Plating System 510(k) February 15, 2013 Section 5 Additional Information - Page 3 of 5
2
Performance Testing
No performance standards applicable to this device have been adopted under Section 514 of the Food. Drug and Cosmetic Act. Performance testing of the NeuroPro® Low Profile Cranial Plating System was conducted in accordance with various international standards and internal Kinamed methods.
All of the NeuroPro® Low Profile components are made of materials which conform to international and/or FDA recognized consensus standards for the type of material. All of these materials have a long successful history in similar neurosurgical implant applications.
The NeuroPro® Low Profile Cranial Plating System was tested as part of design verification/validation to Kinamed test methods with pre-defined acceptance criteria. As applicable, the testing was conducted on the worst case component size and option/design. Bone plates and panels were subjected to bend testing according to ASTM F67-06. Bone screw testing consisted of the following Kinamed test methods:
- · Rate of Insertion (Amount of screw advancement per revolution)
- · Ease of Insertion (Driving torque required per revolution)
- · Torsional Strength
- · Screwdriver Interface Integrity
- · Simulated Use in Animal Bone
The testing met all acceptance criteria and verifies that the performance of the NeuroPro® Low Profile Cranial Plating System is substantially equivalent to the predicate devices.
Basis of Substantial Equivalence
The NeuroPro® Low Profile Cranial Plating System has the following similarities to the standard NeuroPro® Cranial Plating System (K964362) and NeuroPro® Quick Tap® Bone Screws (K982927):
- ·same intended use
- ·same indications for use
- ·same raw material
- ·same method of manufacture
- ·same design
- ·similar sizes and dimensions
- ·same type of mating components
- ·same shelf life
- ·same biocompatibility
- ·same sterilization and packaging methods
The new Low Profile System has some thinner plates/panels, shorter screw head height and is a differentiating color.
3
Conclusion:
The data and information provided in this submission support the conclusion that the NeuroPro® Low Profile Cranial Plating System is substantially equivalent to
its predicate devices, standard NeuroPro® Cranial Plating System and Quick Tap® Bone Screws with respect to intended use, design, and operational principles. The use of low profile components is equivalent to that used in other cleared cranial fixation systems.
NeuroPro® Low Profile Cranial Plating System 510(k) February 15, 2013 Section 5 Additional Information - Page 5 of 5
4
Image /page/4/Picture/2 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States. The seal features a stylized caduceus-like symbol, with three lines curving upwards, representing health and human services. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular pattern around the symbol.
April 5. 2013
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Kinamed. Inc. % Ms. Heather Neely Senior Director of Quality Assurance and Regulatory Compliance 820 Flynn Road Camarillo, CA 93012
Re: K122049
Trade/Device Name: NeuroPro® Low Profile Cranial Plating System Regulation Number: 21 CFR 882.5320 Regulation Name: Preformed alterable cranioplasty plate Regulatory Class: Class II Product Code: GWO, GXR, HBW Dated: February 15, 2013 Received: February 19, 2013
Dear Ms. Neely:
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
5
Page 2 - Ms. Heather Neelv
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 (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 contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree 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 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 Y. Alexander -S
for Victor Krauthamer, Ph.D.
Acting Director Division of Neurological and Physical Medicine Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
6
Indications for Use Statement
510(k) Number (if known): K122049
Device Name: NeuroPro® Low Profile Cranial Plating System
Indications for Use:
The NeuroPro® Low Profile Cranial Plating System Family is intended for:
-
- Internal fixation of fractures and osteotomies of the cranial skeleton.
-
- Internal fixation of cranial bone flap osteotomies.
- Reconstruction of bony defects and deficits in the cranial skeleton.
The NeuroPro® Low Profile Cranial Plating System is not indicated for use in the spine or high load bearing applications.
Prescription Use X AND/OR Over-The-Counter Use_
(21 CFR 801 Subpart C) (Part 21 CFR 801 Subpart D)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Image /page/6/Picture/12 description: The image shows the name "Tieuvi H. Nguyen" in bold, black font. Below the name is the date and time "2013.04.05 13:35:35 -04'00'" also in bold, black font. The text is surrounded by a decorative border.
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(Division Sign Off) Division of Neurological and Physical Medicine Devices (DNPMD) 510(k) Number _K122049