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FDA 510(k)

HERITAGE SPECIAL ALLOY

K-Number: K771110 · 1977-07-15

ApplicantHowmedica Corp.
Decision Date1977-07-15
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HERITAGE SPECIAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K771110. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERITAGE SPECIAL ALLOY?

HERITAGE SPECIAL ALLOY is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Howmedica Corp.. The 510(k) number is K771110.

When did HERITAGE SPECIAL ALLOY receive FDA 510(k) clearance?

HERITAGE SPECIAL ALLOY received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771110.

Who is the listed applicant for HERITAGE SPECIAL ALLOY?

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

What is the FDA product code for HERITAGE SPECIAL ALLOY?

The FDA product code for HERITAGE SPECIAL ALLOY is EJT.

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Other records listing Howmedica Corp. as applicant

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Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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