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FDA 510(k)

EAGLE + ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K070994 · 2007-05-09

ApplicantDepuy Spine, Inc.
Decision Date2007-05-09
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EAGLE + ANTERIOR CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Spine, Inc.. It received FDA 510(k) clearance on 2007-05-09 under 510(k) number K070994. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE + ANTERIOR CERVICAL PLATE SYSTEM?

EAGLE + ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-05-09. The listed applicant is Depuy Spine, Inc.. The 510(k) number is K070994.

When did EAGLE + ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

EAGLE + ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2007-05-09, under 510(k) number K070994.

Who is the listed applicant for EAGLE + ANTERIOR CERVICAL PLATE SYSTEM?

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

What is the FDA product code for EAGLE + ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for EAGLE + ANTERIOR CERVICAL PLATE SYSTEM is KWQ.

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Other records listing Depuy Spine, Inc. as applicant

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Related Devices (Code: KWQ)

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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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