Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OnPoint Augmented Reality Spine System

K-Number: K241870 · 2024-08-19

Decision Date2024-08-19
Product CodeSBF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

OnPoint Augmented Reality Spine System is the device name listed in this FDA 510(k) record. The listed applicant is Onpoint Surgical, Inc.. It received FDA 510(k) clearance on 2024-08-19 under 510(k) number K241870. The device is classified under product code SBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OnPoint Augmented Reality Spine System?

OnPoint Augmented Reality Spine System is a medical device that received FDA 510(k) clearance on 2024-08-19. The listed applicant is Onpoint Surgical, Inc.. The 510(k) number is K241870.

When did OnPoint Augmented Reality Spine System receive FDA 510(k) clearance?

OnPoint Augmented Reality Spine System received FDA 510(k) clearance on 2024-08-19, under 510(k) number K241870.

Who is the listed applicant for OnPoint Augmented Reality Spine System?

The FDA 510(k) record lists Onpoint Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OnPoint Augmented Reality Spine System?

The FDA product code for OnPoint Augmented Reality Spine System is SBF.

Other records listing Onpoint Surgical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: SBF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.