ANTHRO-MODULAR TOTAL KNEE
K-Number: K834432 · 1984-04-11
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Device Summary
Frequently Asked Questions
What is the ANTHRO-MODULAR TOTAL KNEE?
ANTHRO-MODULAR TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1984-04-11. The listed applicant is Zimmer, Inc.. The 510(k) number is K834432.
When did ANTHRO-MODULAR TOTAL KNEE receive FDA 510(k) clearance?
ANTHRO-MODULAR TOTAL KNEE received FDA 510(k) clearance on 1984-04-11, under 510(k) number K834432.
Who is the listed applicant for ANTHRO-MODULAR TOTAL KNEE?
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 ANTHRO-MODULAR TOTAL KNEE?
The FDA product code for ANTHRO-MODULAR TOTAL KNEE is JWH.
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: JWH)
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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