MAXIM ACCEL KNEE SYSTEM
K-Number: K023546 · 2003-01-17
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Device Summary
Frequently Asked Questions
What is the MAXIM ACCEL KNEE SYSTEM?
MAXIM ACCEL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2003-01-17. The listed applicant is Biomet, Inc.. The 510(k) number is K023546.
When did MAXIM ACCEL KNEE SYSTEM receive FDA 510(k) clearance?
MAXIM ACCEL KNEE SYSTEM received FDA 510(k) clearance on 2003-01-17, under 510(k) number K023546.
Who is the listed applicant for MAXIM ACCEL 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 ACCEL KNEE SYSTEM?
The FDA product code for MAXIM ACCEL 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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