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FDA 510(k)

AVAFLEX VERTEBRAL BALLOON SYSTEM

K-Number: K131824 · 2013-10-03

ApplicantCare Fusion
Decision Date2013-10-03
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AVAFLEX VERTEBRAL BALLOON SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2013-10-03 under 510(k) number K131824. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVAFLEX VERTEBRAL BALLOON SYSTEM?

AVAFLEX VERTEBRAL BALLOON SYSTEM is a medical device that received FDA 510(k) clearance on 2013-10-03. The listed applicant is Care Fusion. The 510(k) number is K131824.

When did AVAFLEX VERTEBRAL BALLOON SYSTEM receive FDA 510(k) clearance?

AVAFLEX VERTEBRAL BALLOON SYSTEM received FDA 510(k) clearance on 2013-10-03, under 510(k) number K131824.

Who is the listed applicant for AVAFLEX VERTEBRAL BALLOON SYSTEM?

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

What is the FDA product code for AVAFLEX VERTEBRAL BALLOON SYSTEM?

The FDA product code for AVAFLEX VERTEBRAL BALLOON SYSTEM is HRX.

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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.

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