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FDA 510(k)

CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM

K-Number: K934756 · 1994-11-08

Decision Date1994-11-08
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1994-11-08 under 510(k) number K934756. 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 CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM?

CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-11-08. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K934756.

When did CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM receive FDA 510(k) clearance?

CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM received FDA 510(k) clearance on 1994-11-08, under 510(k) number K934756.

Who is the listed applicant for CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM?

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

What is the FDA product code for CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM?

The FDA product code for CODMAN ANTERIOR CERVICAL SPINE PLATE SYSTEM is KWQ.

Related Clinical Trials

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.

Other records listing Codman & Shurtleff, 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.

View all 147 devices →

Related Devices (Code: KWQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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