(88 days)
The Quantum Spinal System components are non-cervical spinal fixation devices intended for use as a pedicle screw system (T1 - S2), a posterior hook and sacral/iliac screw fixation system or as an anterolateral fixation system (T8 - L5). Pedicle screw fixation is limited to skeletally mature patients. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma, (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion.
Not Found
This document describes the Quantum Spinal System, a medical device, and its regulatory clearance through the 510(k) pathway. It does not contain information about acceptance criteria or a study that proves the device meets specific performance criteria in the way that an AI/ML device submission would.
The provided text describes a traditional medical device (spinal fixation system) and its substantial equivalence to predicate devices, rather than an AI/ML device with performance metrics like accuracy, sensitivity, or specificity. Therefore, many of the requested fields are not applicable to the information contained in the provided document.
Here's a breakdown of the available information:
1. Table of Acceptance Criteria and Reported Device Performance:
This information is not provided in a quantifiable way typical for AI/ML device performance. The document states:
| Acceptance Criteria (Implied) | Reported Device Performance |
|---|---|
| Conformance to ASTM Standards (Mechanical/Material) | "Testing per recognized ASTM standards was presented." |
| Substantial Equivalence to Predicate Devices | "Comparisons of device performance data, materials, indications and design/function to predicate devices were provided in making a determination of substantial equivalence." |
2. Sample size used for the test set and the data provenance:
- Not applicable / Not provided. This document describes a spinal implant, not a data-driven device that requires a "test set" in the AI/ML sense. The performance data refers to mechanical and material testing, not clinical data sets.
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts:
- Not applicable / Not provided. Ground truth, in the context of AI/ML, refers to labels or diagnoses provided by experts on a dataset. This information is not relevant to the clearance of a spinal implant.
4. Adjudication method for the test set:
- Not applicable / Not provided. Adjudication methods are used in AI/ML studies to resolve disagreements among experts in labeling data. This is not pertinent to the current device.
5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, and the effect size of how much human readers improve with AI vs without AI assistance:
- Not applicable / Not provided. This device is a surgical implant, not an AI-powered diagnostic or assistive tool. Therefore, an MRMC study comparing human readers with and without AI assistance is irrelevant.
6. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done:
- Not applicable / Not provided. There is no algorithm for this device.
7. The type of ground truth used:
- Not applicable / Not provided. The "ground truth" for a spinal implant's safety and effectiveness is established through engineering testing (e.g., biomechanical strength, material compatibility), pre-clinical studies, and clinical experience with similar predicate devices, rather than a "ground truth" for data labeling. The regulatory decision is based on substantial equivalence to predicate devices which have an established safety and effectiveness profile.
8. The sample size for the training set:
- Not applicable / Not provided. This device does not involve machine learning; therefore, there is no "training set."
9. How the ground truth for the training set was established:
- Not applicable / Not provided. As there is no training set for an AI/ML model, this question is not relevant.
In summary: The provided document is a 510(k) summary for a traditional medical device (spinal fixation system). The regulatory review for such devices focuses on demonstrating substantial equivalence to legally marketed predicate devices, primarily through engineering performance data (e.g., mechanical testing conforming to ASTM standards), material safety, and similarity in design and intended use. The concepts of "acceptance criteria" and "study proving device meets acceptance criteria" for AI/ML devices, involving test sets, ground truth, experts, and reader studies, are not applicable to this type of traditional device clearance.
{0}------------------------------------------------
| Summary of Safety and Effectiveness Information | |
|---|---|
| -- | ------------------------------------------------- |
| Sponsor: | Pioneer Surgical Technology375 River Park CircleMarquette, MI 49855(906) 226-4812Contact: Jonathan M. GilbertJUL - 3 2007 |
|---|---|
| Device Name: | Quantum Spinal System |
| Classification Name: | Spinal Interlaminal Fixation Orthosis, Spinal Intervertebral BodyFixation Orthosis, Spondylolisthesis Spinal Fixation Device Systemand Pedicle Screw Spinal System, Class III. |
| Predicate Device: | K041167 - Quantum Spinal System, K070551 - Quantum SpinalSystem, K052151 - Synthes Pangea Monoaxial System, K031175 -Synthes Click'X Monoaxial System |
| Intended Use: | The Quantum Spinal System components are non-cervical spinalfixation devices intended as an adjunct to fusion for use as a pediclescrew (T1-S2), posterior hook (T1 - L5), sacral/iliac screw fixationor as an anterolateral fixation system (T8 - L5). Pedicle screwfixation is limited to skeletally mature patients. These devices areindicated for all of the following indications regardless of theintended use: degenerative disc disease (defined as discogenic backpain with degeneration of the disc confirmed by history andradiographic studies), spondylolisthesis, trauma, (i.e., fracture ordislocation), deformities or curvatures (i.e., scoliosis, kyphosis,and/or lordosis, Scheuermann's Disease), tumor, stenosis,pseudoarthosis, and failed previous fusion. |
| Material: | Materials used to manufacture the implants (titanium alloy) andinstruments (medical grade stainless steel) of this system are inconformance with ASTM Standard Specifications. |
| Performance Data: | Testing per recognized ASTM standards was presented. |
| Performance and SEDetermination: | Comparisons of device performance data, materials, indications anddesign/function to predicate devices were provided in making adetermination of substantial equivalence. |
{1}------------------------------------------------
DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
Image /page/1/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular border with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES · USA" arranged around the perimeter. Inside the circle is a stylized eagle emblem, depicted with flowing lines to suggest movement or flight.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Pioneer Surgical Technology % Mr. Jonathan Gilbert VP, Clinical and Regulatory Affairs 375 River Park Circle Marquette, MI 49855
Re: K070973
Trade/Device Name: OUANTUM Spinal System Regulation Number: 21 CFR 888.3070 Regulation Name: Pedicle screw spinal system Regulatory Class: III Product Code: NKB, KWQ, KWP, MNI, MNH Dated: April 4, 2007 Received: April 6, 2007
Dear Mr. Gilbert:
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. Iisting of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
111 - 3 2007
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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); 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.
{2}------------------------------------------------
Page 2 - Mr. Jonathan Gilbert
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at toll-free number (800) 638-2041 or (240) 276-3150 or the Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Sincerely, yours,
for
Mark N. Melkerson / Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
{3}------------------------------------------------
Indications for Use Statement 2.0
| 510(k) Number (if known): | K070973 |
|---|---|
| Device Name: | Quantum Spinal System |
| Indications for Use: | The Quantum Spinal System components are non-cervical spinalfixation devices intended for use as a pedicle screw system (T1 - S2), aposterior hook and sacral/iliac screw fixation system or as ananterolateral fixation system (T8 - L5). Pedicle screw fixation islimited to skeletally mature patients. These devices are indicated for allof the following indications regardless of the intended use:degenerative disc disease (defined as discogenic back pain withdegeneration of the disc confirmed by history and radiographicstudies), spondylolisthesis, trauma, (i.e., fracture or dislocation),deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis,Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failedprevious fusion. |
Prescription Use
(Per 21 CFR 801.109) √
Over-the-Counter Use _________________________________________________________________________________________________________________________________________________________
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
OR
P.M.
(Division Sign-Off)
(Division Sign-Off) Division of General, Restorative, and Neurological Devices
510(k) Number K070973
Original 4/4/07
Revised 6/8/07
Pioneer Surgical Technology Premarket Notification
N/A