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FDA 510(k)

CAMPION CERVICAL HOOK

K-Number: K891349 · 1989-03-29

Decision Date1989-03-29
Product CodeHDC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CAMPION CERVICAL HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Simpson/Basye, Inc.. It received FDA 510(k) clearance on 1989-03-29 under 510(k) number K891349. The device is classified under product code HDC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPION CERVICAL HOOK?

CAMPION CERVICAL HOOK is a medical device that received FDA 510(k) clearance on 1989-03-29. The listed applicant is Simpson/Basye, Inc.. The 510(k) number is K891349.

When did CAMPION CERVICAL HOOK receive FDA 510(k) clearance?

CAMPION CERVICAL HOOK received FDA 510(k) clearance on 1989-03-29, under 510(k) number K891349.

Who is the listed applicant for CAMPION CERVICAL HOOK?

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

What is the FDA product code for CAMPION CERVICAL HOOK?

The FDA product code for CAMPION CERVICAL HOOK is HDC.

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 Simpson/Basye, 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 12 devices →

Related Devices (Code: HDC)

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

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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