T-PLATE
K-Number: K931692 · 1994-05-04
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Device Summary
Frequently Asked Questions
What is the T-PLATE?
T-PLATE is a medical device that received FDA 510(k) clearance on 1994-05-04. The listed applicant is Onyx Medical Corp.. The 510(k) number is K931692.
When did T-PLATE receive FDA 510(k) clearance?
T-PLATE received FDA 510(k) clearance on 1994-05-04, under 510(k) number K931692.
Who is the listed applicant for T-PLATE?
The FDA 510(k) record lists Onyx Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T-PLATE?
The FDA product code for T-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 Onyx Medical Corp. 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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