Universal Pilot Guidance Instrument System
FDA 510(k) K213491 · Ctl Medical Corporation
510(k) numberK213491
Submission
- Device name
- Universal Pilot Guidance Instrument System
- Applicant
- Ctl Medical Corporation
Addison, TX, US - Received
- November 1, 2021
- Decision date
- May 12, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- OLO – Orthopedic Stereotaxic Instrument
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 882.4560
- Specialty
- Neurology
Stereotaxic guidance during orthopedic surgery procedures. Indicated for Orthopedic joint or spine surgery. Neurological stereotaxic instruments are classified under product code HAW.
Other 510(k)s with product code OLO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262506 | Remex Spine Surgery Navigation - Universal InstrumentsOLO · Special | Remex Medical Corp. | 08/20/2026SE |
| K261410 | Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration…OLO · Traditional | Suite 201, National Innovation Centre | 07/30/2026SE |
| K261205 | SPINEART Navigation Instrument SystemOLO · Traditional | Spineart SA | 07/29/2026SE |
| K262121 | Ion-L Navigated InstrumentsOLO · Special | SurGenTec, LLC | 07/24/2026SE |
| K261024 | TMINI Miniature Robotic SystemOLO · Traditional | THINK Surgical, Inc. | 07/24/2026SE |
| K261113 | Op.n Spine Navigation and Robotic GuidanceOLO · Traditional | Ecential Robotics | 07/22/2026SE |
| K261852 | OTS HipOLO · Special | Ortoma AB | 07/01/2026SE |
| K253921 | VERTICALE® Navigation InstrumentsOLO · Traditional | Silony Medical GmbH | 06/26/2026SE |
| K260480 | VELYS Robotic-Assisted SolutionOLO · Traditional | Depuy Ireland UC | 06/25/2026SE |
| K260369 | Dynamis Robotic Surgical SystemOLO · Traditional | LEM Surgical AG | 06/20/2026SE |
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| K231359 | RODIN Expandable Lumbar Cage SystemMAX · Special | 06/09/2023SE |
| K220513 | NITRO Interbody Fusion Cage System FamilyODP · Traditional | 04/25/2023SE |
| K220334 | MONET Anterior Cervical Plate SystemKWQ · Traditional | 11/09/2022SE |
| K211785 | CASSATT SIJ Fixation SystemOUR · Traditional | 10/17/2022SE |
| K213641 | MONDRIAN ALIF Cage with Supplementary Fixation PlateMAX · Traditional | 09/15/2022SE |
| K192863 | MONDRIAN Lumbar Interbody Fusion Cage SystemMAX · Traditional | 08/26/2020SE |
| K182151 | MONET Anterior Cervical Interbody Fusion Cage System with Supplementary Fixation PlateOVE · Traditional | 10/11/2018SE |
| K172788 | MONET Anterior Cervical Interbody Fusion Cage SystemODP · Traditional | 06/25/2018SE |
Questions and answers
When was Universal Pilot Guidance Instrument System cleared by the FDA?
Universal Pilot Guidance Instrument System (K213491) received a 510(k) decision of Substantially Equivalent on May 12, 2022, 192 days after the submission was received.
What is the product code of K213491?
The FDA product code is OLO – Orthopedic Stereotaxic Instrument, a Class II (moderate risk) device regulated under 21 CFR 882.4560.