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

FDA 510(k)

Beactive Brace

K-Number: K151476 · 2016-02-26

ApplicantNatures Pillows, Inc.
Decision Date2016-02-26
Product CodePMV
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Beactive Brace is a medical device manufactured by Natures Pillows, Inc.. It received FDA 510(k) clearance on 2016-02-26 under approval number K151476. The device is classified under product code PMV. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Beactive Brace?

Beactive Brace is a medical device that received FDA 510(k) clearance on 2016-02-26. It is manufactured by Natures Pillows, Inc.. The 510(k) number is K151476.

When was Beactive Brace approved by the FDA?

Beactive Brace received FDA 510(k) clearance on 2016-02-26, under approval number K151476.

What company makes Beactive Brace?

Beactive Brace is manufactured by Natures Pillows, Inc..

What is the FDA product code for Beactive Brace?

The FDA product code for Beactive Brace is PMV.

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.

↑