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FDA 510(k)

SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE

K-Number: K926453 · 1993-10-12

ApplicantSynthes (Usa)
Decision Date1993-10-12
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K926453. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE?

SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Synthes (Usa). The 510(k) number is K926453.

When did SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE receive FDA 510(k) clearance?

SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE received FDA 510(k) clearance on 1993-10-12, under 510(k) number K926453.

Who is the listed applicant for SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE?

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 (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE?

The FDA product code for SYNTHES (U.S.A.) ANTERIOR CERVICAL VERTEBRAE PLATE is KWQ.

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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.

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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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