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FDA 510(k)

VITOSS-FILLED CARTRIDGE

K-Number: K032130 · 2003-11-05

ApplicantOrthovita, Inc.
Decision Date2003-11-05
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VITOSS-FILLED CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Orthovita, Inc.. It received FDA 510(k) clearance on 2003-11-05 under 510(k) number K032130. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITOSS-FILLED CARTRIDGE?

VITOSS-FILLED CARTRIDGE is a medical device that received FDA 510(k) clearance on 2003-11-05. The listed applicant is Orthovita, Inc.. The 510(k) number is K032130.

When did VITOSS-FILLED CARTRIDGE receive FDA 510(k) clearance?

VITOSS-FILLED CARTRIDGE received FDA 510(k) clearance on 2003-11-05, under 510(k) number K032130.

Who is the listed applicant for VITOSS-FILLED CARTRIDGE?

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

What is the FDA product code for VITOSS-FILLED CARTRIDGE?

The FDA product code for VITOSS-FILLED CARTRIDGE is MQV.

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Related Devices (Code: MQV)

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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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