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FDA 510(k)

PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP

K-Number: K853205 · 1985-09-16

ApplicantDepuy, Inc.
Decision Date1985-09-16
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1985-09-16 under 510(k) number K853205. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP?

PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Depuy, Inc.. The 510(k) number is K853205.

When did PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP receive FDA 510(k) clearance?

PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853205.

Who is the listed applicant for PROXIMAL POROCOAT MODIFIED MEDICAL ASPECT AML HIP?

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

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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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