BIOMET CALCANEAL PLATE
K-Number: K022515 · 2002-09-17
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Device Summary
Frequently Asked Questions
What is the BIOMET CALCANEAL PLATE?
BIOMET CALCANEAL PLATE is a medical device that received FDA 510(k) clearance on 2002-09-17. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K022515.
When did BIOMET CALCANEAL PLATE receive FDA 510(k) clearance?
BIOMET CALCANEAL PLATE received FDA 510(k) clearance on 2002-09-17, under 510(k) number K022515.
Who is the listed applicant for BIOMET CALCANEAL PLATE?
The FDA 510(k) record lists Biomet Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOMET CALCANEAL PLATE?
The FDA product code for BIOMET CALCANEAL PLATE is HRS.
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 Orthopedics, 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: HRS)
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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