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FDA 510(k)

BENVENUE VCF OSTEO COIL SYSTEM

K-Number: K070293 · 2007-07-10

ApplicantBenvenue Medical, Inc.
Decision Date2007-07-10
Product CodeOCJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BENVENUE VCF OSTEO COIL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Benvenue Medical, Inc.. It received FDA 510(k) clearance on 2007-07-10 under 510(k) number K070293. The device is classified under product code OCJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENVENUE VCF OSTEO COIL SYSTEM?

BENVENUE VCF OSTEO COIL SYSTEM is a medical device that received FDA 510(k) clearance on 2007-07-10. The listed applicant is Benvenue Medical, Inc.. The 510(k) number is K070293.

When did BENVENUE VCF OSTEO COIL SYSTEM receive FDA 510(k) clearance?

BENVENUE VCF OSTEO COIL SYSTEM received FDA 510(k) clearance on 2007-07-10, under 510(k) number K070293.

Who is the listed applicant for BENVENUE VCF OSTEO COIL SYSTEM?

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

What is the FDA product code for BENVENUE VCF OSTEO COIL SYSTEM?

The FDA product code for BENVENUE VCF OSTEO COIL SYSTEM is OCJ.

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Official Source

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