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FDA 510(k)

COROENT INTERLOCK SYSTEM

K-Number: K102547 · 2011-02-07

ApplicantNuvasive, Inc.
Decision Date2011-02-07
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COROENT INTERLOCK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2011-02-07 under 510(k) number K102547. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COROENT INTERLOCK SYSTEM?

COROENT INTERLOCK SYSTEM is a medical device that received FDA 510(k) clearance on 2011-02-07. The listed applicant is Nuvasive, Inc.. The 510(k) number is K102547.

When did COROENT INTERLOCK SYSTEM receive FDA 510(k) clearance?

COROENT INTERLOCK SYSTEM received FDA 510(k) clearance on 2011-02-07, under 510(k) number K102547.

Who is the listed applicant for COROENT INTERLOCK SYSTEM?

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

What is the FDA product code for COROENT INTERLOCK SYSTEM?

The FDA product code for COROENT INTERLOCK SYSTEM is OVE.

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Other records listing Nuvasive, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: OVE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K263049SABER-C SystemElevation SpineK261882Pisces-SC Standalone Cervical Interbody SystemOsseus Fusions Systems, LLCK261451ZSAlign Cervical Interbody SystemZSFab, Inc.K262094E3D™-C Interbody SystemEvolution SpineK261279DeltaNEC Interbody SystemNexus SpineK252982CONDUIT™ ZERO-P™ VA Secured Spacer SystemAvalign Technologies, Inc.

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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