TOTAL HIP, NEW ENGLAND BAPTIST
K-Number: K780329 · 1978-03-17
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Device Summary
Frequently Asked Questions
What is the TOTAL HIP, NEW ENGLAND BAPTIST?
TOTAL HIP, NEW ENGLAND BAPTIST is a medical device that received FDA 510(k) clearance on 1978-03-17. The listed applicant is Depuy, Inc.. The 510(k) number is K780329.
When did TOTAL HIP, NEW ENGLAND BAPTIST receive FDA 510(k) clearance?
TOTAL HIP, NEW ENGLAND BAPTIST received FDA 510(k) clearance on 1978-03-17, under 510(k) number K780329.
Who is the listed applicant for TOTAL HIP, NEW ENGLAND BAPTIST?
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 TOTAL HIP, NEW ENGLAND BAPTIST?
The FDA product code for TOTAL HIP, NEW ENGLAND BAPTIST is JDG.
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 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.
Related Devices (Code: JDG)
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
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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