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)

VIVORTE BVF

K-Number: K130703 · 2013-09-12

ApplicantVivorte, Inc.
Decision Date2013-09-12
Product CodeMBP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VIVORTE BVF is the device name listed in this FDA 510(k) record. The listed applicant is Vivorte, Inc.. It received FDA 510(k) clearance on 2013-09-12 under 510(k) number K130703. The device is classified under product code MBP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVORTE BVF?

VIVORTE BVF is a medical device that received FDA 510(k) clearance on 2013-09-12. The listed applicant is Vivorte, Inc.. The 510(k) number is K130703.

When did VIVORTE BVF receive FDA 510(k) clearance?

VIVORTE BVF received FDA 510(k) clearance on 2013-09-12, under 510(k) number K130703.

Who is the listed applicant for VIVORTE BVF?

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

What is the FDA product code for VIVORTE BVF?

The FDA product code for VIVORTE BVF is MBP.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vivorte, 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.

K131133VIVORTE BVF LITE

Related Devices (Code: MBP)

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.

K242799PliaFX FloLifenet HealthK130498OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTYBacterin International, Inc.K122513CLEARED UNDER GRAFTON II EDBMMedtronic Sofamor Danek, Inc.K113728SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTYHans Biomed Corp.K103742ACCELL EVO3 (FORMERLY ACCELL A2I)Integra Life SciencesK091193ACCELL EVO3CIsotis Orthobiologics, Inc.

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.

↑