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FDA 510(k)

OSTEOCURE RESORBABLE BEAD KIT

K-Number: K051406 · 2005-08-01

ApplicantNexa Orthopedics, Inc.
Decision Date2005-08-01
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOCURE RESORBABLE BEAD KIT is the device name listed in this FDA 510(k) record. The listed applicant is Nexa Orthopedics, Inc.. It received FDA 510(k) clearance on 2005-08-01 under 510(k) number K051406. 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 OSTEOCURE RESORBABLE BEAD KIT?

OSTEOCURE RESORBABLE BEAD KIT is a medical device that received FDA 510(k) clearance on 2005-08-01. The listed applicant is Nexa Orthopedics, Inc.. The 510(k) number is K051406.

When did OSTEOCURE RESORBABLE BEAD KIT receive FDA 510(k) clearance?

OSTEOCURE RESORBABLE BEAD KIT received FDA 510(k) clearance on 2005-08-01, under 510(k) number K051406.

Who is the listed applicant for OSTEOCURE RESORBABLE BEAD KIT?

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

What is the FDA product code for OSTEOCURE RESORBABLE BEAD KIT?

The FDA product code for OSTEOCURE RESORBABLE BEAD KIT is 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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