(112 days)
The Prase-C Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine (C2-C7). The System is indicated for use in the immobilization of the spine as an adjunct to fusions in patients with: · degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), · spondylolisthesis, · trauma (i.e. fractures or dislocations), · tumors, · deformity (defined as kyphosis, lordosis, or scoliosis), · pseudoarthrosis, · failed previous fusion, · spinal stenosis.
The Prase-C Anterior Cervical Plate System is composed of plates, screws and lockers which are made from titanium alloy Ti-6AI-4V ELI as per ASTM F136. The plates are offered in one-level, two-level, three-level, four-level, five-level fusion configurations. In addition, one level plate consists of a four hole for screw insertion and a two-hole and three-hole for screw insertion. The plate lockers are fixed into the main plate body by rivet technique. The screw type consists of single and double thread and fixed and variable type. This device is supplied non-sterile.
I am sorry, but based on the provided document, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria with the requested details.
The document is an FDA 510(k) clearance letter for a medical device called the "Prase-C Anterior Cervical Plate System." While it mentions "Performance Testing" according to ASTM F1717, it does not provide any specific acceptance criteria (numerical values or performance thresholds) nor does it report detailed device performance data (e.g., specific loads applied, displacements, or number of cycles achieved).
In essence, the document confirms that the device was tested per a standard and found to be "substantially equivalent" to predicate devices, but it does not disclose the actual test results or the pre-defined target values for those results.
Therefore, I cannot populate the table or provide the requested information regarding sample size, data provenance, expert ground truth, adjudication methods, multi-reader multi-case studies, standalone performance, or training set details, as this information is not present in the provided text.
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GBS Commonwealth Co., Ltd. Jimmy Kim RA C-309, Woolim Lion's Valley, 168, Gasan Digital 1-ro Geumcheon-gu, Seoul 08507 Korea, South
Re: K211205
Trade/Device Name: Prase-C Anterior Cervical Plate System Regulation Number: 21 CFR 888.3050 Regulation Name: Spinal Interlaminal Fixation Orthosis Regulatory Class: Class II Product Code: KWP Dated: June 17, 2021 Received: June 21, 2021
Dear Jimmy Kim:
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 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
August 12, 2021
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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 (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,
for
Colin O'Neill, M.B.E. Assistant Director DHT6B: Division of Spinal Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K211205
Device Name
Prase-C Anterior Cervical Plate System
Indications for Use (Describe)
The Prase-C Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine (C2-C7). The System is indicated for use in the immobilization of the spine as an adjunct to fusions in patients with: · degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by
- patient history and radiographic studies),
- · spondylolisthesis,
- · trauma (i.e. fractures or dislocations),
- · tumors,
- · deformity (defined as kyphosis, lordosis, or scoliosis),
- · pseudoarthrosis,
- · failed previous fusion,
- · spinal stenosis.
| Type of Use (Select one or both, as applicable) | |
|---|---|
X | Prescription Use (Part 21 CFR 801 Subpart D)
| | Over-The-Counter Use (21 CFR 801 Subpart C)
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Image /page/3/Picture/1 description: The image shows the logo for GBS Commonwealth. The letters "GBS" are in large, bold, blue font. Below the letters is the word "COMMONWEALTH" in a smaller, bold, blue font. The background of the logo is a light gray oval shape.
510(k) SUMMARY
The following summary is being submitted as required by 21 CFR 807.92(a):
1. Device Identification
| Submitter: | GBS Commonwealth Co., Ltd.#C-309, 168 Gasan Digital 1-ro, Geumcheon-Gu Seoul,South KoreaPhone. 82-2-6925-4469e-mail: Jimmy.kim@gbscommonwealth.com |
|---|---|
| Contact Person: | Jimmy Kim |
| Date prepared | April, 13, 2021 |
| Trade Name | Prase-C Anterior Cervical Plate System |
|---|---|
| Regulatory Class | Class II |
| RegulationName/Common Name | Anterior Cervical Plate |
| Classification Name | Spinal Intervertebral body fixation orthosis(21 CFR 888.3060) |
| Panel | Orthopedic |
| Product Code | KWQ |
2. Purpose of 510(k)
The GBS Commonwealth Co. Ltd., here by submits this special submission : for original product Introduction of Prase-C Anterior Cervical Plate System
3. Predicate or legally marketed devices which are substantially equivalent
-
- Primary Predicate Device: : K202878 Prase-C Anterior Cervical Plate System
-
- Additional Predicated(s) : (1) K191584 Fortico Anterior Cervical Fixation System
(2) K182418 V3 Segmental Plating System
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Image /page/4/Picture/1 description: The image shows the logo for GBS Commonwealth. The letters "GBS" are in large, bold, blue font. Below the letters is the word "COMMONWEALTH" in a smaller, bold, blue font. The background of the logo is a globe.
4. Description of the Device
The Prase-C Anterior Cervical Plate System is composed of plates, screws and lockers which are made from titanium alloy Ti-6AI-4V ELI as per ASTM F136. The plates are offered in one-level, two-level, three-level, four-level, five-level fusion configurations. In addition, one level plate consists of a four hole for screw insertion and a two-hole and three-hole for screw insertion. The plate lockers are fixed into the main plate body by rivet technique. The screw type consists of single and double thread and fixed and variable type. This device is supplied non-sterile.
5. Indication for Use
The Prase-C Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine (C2-C7). The System is indicated for use in the immobilization and stabilization of the spine as an adjunct to fusions in patients with:
- . degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies),
- spondylolisthesis,
- . trauma (i.e. fractures or dislocations),
- tumors,
- deformity (defined as kyphosis, lordosis, or scoliosis),
- . pseudoarthrosis,
- failed previous fusion, ●
- . spinal stenosis.
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Image /page/5/Picture/1 description: The image shows the logo for GBS Commonwealth. The letters "GBS" are in large, bold, blue font. Below the letters is the word "COMMONWEALTH" in a smaller, bold, blue font. The background is white.
- Comparison of the technological characteristics of the subject and predicate 6. devices
The Prase-C Anterior Cervical Plate System is considered substantially equivalent to the primary predicate Prase-C Anterior Cervical Plate System K202878, Fortico Anterior Carvical Fixation System (K191584) and V3 Segmental Plating System (K182418). They are similar in design, material, scientific technologies and indications for use.
7. Performance Testing
Static compression bending, Static torsion and Fatigue compression bending test were performed according to ASTM F1717 on a worst-case, cervical plate construct.
8. Conclusion
The Prase-C Anterior Cervical Plate System is substantially equivalent to legally marketed predicates.
§ 888.3060 Spinal intervertebral body fixation orthosis.
(a)
Identification. A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct “sway back,” scoliosis (lateral curvature of the spine), or other conditions.(b)
Classification. Class II.