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FDA 510(k)

KNEE COMPRESSION HOOK SYSTEM

K-Number: K790465 · 1979-04-12

ApplicantZimmer, Inc.
Decision Date1979-04-12
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KNEE COMPRESSION HOOK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1979-04-12 under 510(k) number K790465. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNEE COMPRESSION HOOK SYSTEM?

KNEE COMPRESSION HOOK SYSTEM is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Zimmer, Inc.. The 510(k) number is K790465.

When did KNEE COMPRESSION HOOK SYSTEM receive FDA 510(k) clearance?

KNEE COMPRESSION HOOK SYSTEM received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790465.

Who is the listed applicant for KNEE COMPRESSION HOOK SYSTEM?

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

What is the FDA product code for KNEE COMPRESSION HOOK SYSTEM?

The FDA product code for KNEE COMPRESSION HOOK SYSTEM is KWP.

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 Zimmer, 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.

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Related Devices (Code: KWP)

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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