GALANTE FIBER METAL TOTAL HIP
K-Number: K833912 · 1983-12-22
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Device Summary
Frequently Asked Questions
What is the GALANTE FIBER METAL TOTAL HIP?
GALANTE FIBER METAL TOTAL HIP is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Zimmer, Inc.. The 510(k) number is K833912.
When did GALANTE FIBER METAL TOTAL HIP receive FDA 510(k) clearance?
GALANTE FIBER METAL TOTAL HIP received FDA 510(k) clearance on 1983-12-22, under 510(k) number K833912.
Who is the listed applicant for GALANTE FIBER METAL TOTAL HIP?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GALANTE FIBER METAL TOTAL HIP?
The FDA product code for GALANTE FIBER METAL TOTAL HIP is JDI.
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 Zimmer, 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: JDI)
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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