MAXIM KNEE SYSTEM
K-Number: K993159 · 1999-10-14
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Device Summary
Frequently Asked Questions
What is the MAXIM KNEE SYSTEM?
MAXIM KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Biomet, Inc.. The 510(k) number is K993159.
When did MAXIM KNEE SYSTEM receive FDA 510(k) clearance?
MAXIM KNEE SYSTEM received FDA 510(k) clearance on 1999-10-14, under 510(k) number K993159.
Who is the listed applicant for MAXIM KNEE SYSTEM?
The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXIM KNEE SYSTEM?
The FDA product code for MAXIM KNEE SYSTEM 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 Biomet, 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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