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FDA 510(k)

HOOK HOLLER

K-Number: K770759 · 1977-04-29

ApplicantDepuy, Inc.
Decision Date1977-04-29
Product CodeKIK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOOK HOLLER is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-04-29 under 510(k) number K770759. The device is classified under product code KIK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOK HOLLER?

HOOK HOLLER is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Depuy, Inc.. The 510(k) number is K770759.

When did HOOK HOLLER receive FDA 510(k) clearance?

HOOK HOLLER received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770759.

Who is the listed applicant for HOOK HOLLER?

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

What is the FDA product code for HOOK HOLLER?

The FDA product code for HOOK HOLLER is KIK.

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Other records listing Depuy, 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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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