TRIMED BONE PLATES
K-Number: K060041 · 2006-02-07
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Device Summary
Frequently Asked Questions
What is the TRIMED BONE PLATES?
TRIMED BONE PLATES is a medical device that received FDA 510(k) clearance on 2006-02-07. The listed applicant is TriMed, Inc.. The 510(k) number is K060041.
When did TRIMED BONE PLATES receive FDA 510(k) clearance?
TRIMED BONE PLATES received FDA 510(k) clearance on 2006-02-07, under 510(k) number K060041.
Who is the listed applicant for TRIMED BONE PLATES?
The FDA 510(k) record lists TriMed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIMED BONE PLATES?
The FDA product code for TRIMED BONE PLATES 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 TriMed, 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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