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)

xvision Spine system (XVS)

K-Number: K211188 · 2021-07-19

Decision Date2021-07-19
Product CodeSBF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

xvision Spine system (XVS) is the device name listed in this FDA 510(k) record. The listed applicant is Augmedics, Ltd.. It received FDA 510(k) clearance on 2021-07-19 under 510(k) number K211188. 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 xvision Spine system (XVS)?

xvision Spine system (XVS) is a medical device that received FDA 510(k) clearance on 2021-07-19. The listed applicant is Augmedics, Ltd.. The 510(k) number is K211188.

When did xvision Spine system (XVS) receive FDA 510(k) clearance?

xvision Spine system (XVS) received FDA 510(k) clearance on 2021-07-19, under 510(k) number K211188.

Who is the listed applicant for xvision Spine system (XVS)?

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

What is the FDA product code for xvision Spine system (XVS)?

The FDA product code for xvision Spine system (XVS) is SBF.

Other records listing Augmedics, Ltd. 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.

View all 7 devices →

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.