SPOON PLATE
K-Number: K931690 · 1994-06-07
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Device Summary
Frequently Asked Questions
What is the SPOON PLATE?
SPOON PLATE is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Onyx Medical Corp.. The 510(k) number is K931690.
When did SPOON PLATE receive FDA 510(k) clearance?
SPOON PLATE received FDA 510(k) clearance on 1994-06-07, under 510(k) number K931690.
Who is the listed applicant for SPOON 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 SPOON PLATE?
The FDA product code for SPOON 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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