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FDA 510(k)

RESURFACE PROSTHESES FOR HIP JOINT

K-Number: K761324 · 1977-01-05

ApplicantHolco Instrument Corp.
Decision Date1977-01-05
Product CodeKXA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RESURFACE PROSTHESES FOR HIP JOINT is the device name listed in this FDA 510(k) record. The listed applicant is Holco Instrument Corp.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761324. The device is classified under product code KXA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESURFACE PROSTHESES FOR HIP JOINT?

RESURFACE PROSTHESES FOR HIP JOINT is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Holco Instrument Corp.. The 510(k) number is K761324.

When did RESURFACE PROSTHESES FOR HIP JOINT receive FDA 510(k) clearance?

RESURFACE PROSTHESES FOR HIP JOINT received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761324.

Who is the listed applicant for RESURFACE PROSTHESES FOR HIP JOINT?

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

What is the FDA product code for RESURFACE PROSTHESES FOR HIP JOINT?

The FDA product code for RESURFACE PROSTHESES FOR HIP JOINT is KXA.

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.

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Other records listing Holco Instrument Corp. 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.

K770428VARIOUS SURG. & DIAGNOSTIC INSTRU. ETC.

Related Devices (Code: KXA)

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.

K201219Biocore9 Femoral Head Resurfacing ComponentBiocore9, LLCK092198CORMET CEMENTLESS RESURFACING FEMORAL HEADCorin USAK082673CONSERVE PRESSFIT FEMORAL COMPONENTWrightmedicaltechnologyincK071053RECAP HA PRESS-FIT FEMORAL RESURFACING HEADBiomet, Inc.K070292DUROM HIP RESURFACING SYSTEM, FEMORAL COMPONENTSZimmer GmbHK062960CONSERVE FEMORAL RESURFACING COMPONENTWrightmedicaltechnologyinc

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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