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FDA 510(k)

SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM

K-Number: K945700 · 1995-07-20

ApplicantSynthes (Usa)
Decision Date1995-07-20
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1995-07-20 under 510(k) number K945700. 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 SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM?

SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-20. The listed applicant is Synthes (Usa). The 510(k) number is K945700.

When did SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM receive FDA 510(k) clearance?

SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM received FDA 510(k) clearance on 1995-07-20, under 510(k) number K945700.

Who is the listed applicant for SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM?

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

What is the FDA product code for SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM?

The FDA product code for SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE 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 Synthes (Usa) 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: 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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