← Product Code MRW · K092464 # SPINEOLOGY FACET SCREW (K092464) _Spineology, Inc. · MRW · Nov 9, 2009 · OR · SESE_ **Canonical URL:** https://fda.innolitics.com/device/K092464 ## Device Facts - **Applicant:** Spineology, Inc. - **Product Code:** MRW - **Decision Date:** Nov 9, 2009 - **Decision:** SESE - **Submission Type:** Traditional - **Device Class:** Class U - **Review Panel:** OR - **Attributes:** Therapeutic ## Intended Use The Spineology Facet Screw System is intended to stabilize the spine as an aid to fusion by transfacet fixation. The device is indicated for posterior surgical treatment of any or all of the following at the L1 to S1 (inclusive) spinal levels: Spondylolisthesis, Pseudoarthrosis or failed previous fusions which are symptomatic; Degenerative Disc Disease (DDD) as defined by back pain of discogenic origin with degeneration of disc confirmed by history and radiographic studies and/or degenerative disease of the facets with instability. ## Device Story The Spineology Facet Screw System is a spinal fixation device used by surgeons to stabilize the lumbar spine. It consists of cannulated screws, available in partially or fully threaded configurations, designed for bilateral transfacet fixation. The device is implanted during posterior spinal surgery to aid in fusion. By providing mechanical stability to the facet joints, the system helps alleviate symptoms associated with spinal instability, such as those caused by degenerative disc disease or failed prior fusions. The device is intended for use in a clinical/surgical setting. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Cannulated screws; medical grade titanium alloy (ASTM F-136); bilateral transfacet fixation; various lengths; partially or fully threaded. ## Predicate Devices - ChameleonTM Fixation System ([K071420](/device/K071420.md)) - TranS1 Facet Screws ([K073515](/device/K073515.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}------------------------------------------------ K092464 Page 1 of 1 | Appendix C | NOV - 9 2009 | | |-------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--| | | 510(k) Summary | | | Applicant: | Spineology Inc.
7200 Hudson Blvd North
Suite 205
St Paul, MN 55128-7055
Phone: 651-256-8500
Fax: 651-256-8505 | | | Contact Person: | Karen Roche | | | Date Prepared: | August 3, 2009 | | | Trade Name: | Spineology Facet Screw System | | | Product
Classification and
Code: | Unclassified, Product Code MRW | | | Predicate Device(s): | K071420 ChameleonTM Fixation System (SpineFrontierTM, Inc.)
K073515 TranS1 Facet Screws (TranS1, ® Inc.) | | | Device Description: | The Spineology Facet Screw System is designed to provide bilateral
transfacet fixation of the lumbar facet joints. The cannulated screw
is available partially or fully threaded in a range of lengths and is
made from medical grade titanium alloy that complies with ASTM
F-136. | | | Intended Use: | The Spineology Facet Screw System is intended to stabilize the
spine as an aid to fusion by transfacet fixation.
The device is indicated for posterior surgical treatment of
any or all of the following at the L1 to S1 (inclusive) spinal
levels: Spondylolisthesis, Pseudoarthrosis or failed previous
fusions which are symptomatic; Degenerative Disc Disease
(DDD) as defined by back pain of discogenic origin with
degeneration of disc confirmed by history and radiographic
studies and/or degenerative disease of the facets with
instability. | | | Summary of
Technological
Characteristics: | The device is shown to be substantially equivalent to the intended
use, materials, configuration, and performance characteristics of the
predicate products. | | | Conclusion: | The information submitted in this premarket notification supports a
determination that the Spineology Facet Screw System is
substantially equivalent in technological characteristics and
intended use to the predicate devices. | | NOV - 9 2009 {1}------------------------------------------------ Image /page/1/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of two main elements: a circular text element and an emblem. The text element reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular fashion. The emblem is a stylized depiction of an eagle, with its wings spread and head turned to the right. Food and Drug Administration 10903 New Hampshire Avenue Document Control Room W-O66-0609 Silver Spring, MD 20993-0002 Spineology, Inc. % Ms. Karen Roche, Vice President Operations and Technology 7200 Hudson Boulevard, N., Suite 205 Saint Paul, Minnesota 55128-7055 Re: K092464 Trade/Device Name: Spineology Facet Screw System Regulation Number: N/A Regulation Name: N/A Regulatory Class: Unclassified Product Code: MRW Dated: August 3, 2009 Received: August 11, 2009 Dear Ms. Roche: 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. NOV - 9 2009 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 {2}------------------------------------------------ ## Page 2 - Ms. Karen Roche device-related adverse events) (21 CFR 803); 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. 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/cdrh/mdr/ 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/cdrh/industry/support/index.html. Sincerely yours. Sincerely yours, Mark H. Millbern Mark N. Melkerson Director Division of Surgical, Orthopedic and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## Appendix D Indications for Use Form Device Name: Spineology Facet Screw System ## Indications for Use: The Spineology Facet Screw System is intended to stabilize the spine as an aid to fusion by transfacet fixation. The device is indicated for posterior surgical treatment of any or all of the following at the L1 to S1 (inclusive) spinal levels: Spondylolisthesis, Pseudoarthrosis or failed previous fusions which are symptomatic; Degenerative Disc Disease (DDD) as defined by back pain of discogenic origin with degeneration of disc confirmed by history and radiographic studies and/or degenerative disease of the facets with instability. | Prescription Use | X | |-----------------------------|---| | (Part 21 CFR 801 Subpart D) | | AND/OR | Over-The-Counter Use | | |------------------------|--| | (21 CFR 801 Subpart C) | | (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) .. ... ・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・・ ・・ :::: . :: . : '' : : . "::::: . . . : : : Concurrence of CDRH, Office of Device Evaluation (ODE) Mark N. Milliken (Division Sign-Off) Division of Surgical, Orthopedic, and Restorative Devices 510(k) Number K092464 --- **Source:** [https://fda.innolitics.com/device/K092464](https://fda.innolitics.com/device/K092464) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com