ULNAR FRACTURE BRACE
K-Number: K802908 · 1980-12-17
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Device Summary
Frequently Asked Questions
What is the ULNAR FRACTURE BRACE?
ULNAR FRACTURE BRACE is a medical device that received FDA 510(k) clearance on 1980-12-17. The listed applicant is Orthomedics. The 510(k) number is K802908.
When did ULNAR FRACTURE BRACE receive FDA 510(k) clearance?
ULNAR FRACTURE BRACE received FDA 510(k) clearance on 1980-12-17, under 510(k) number K802908.
Who is the listed applicant for ULNAR FRACTURE BRACE?
The FDA 510(k) record lists Orthomedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULNAR FRACTURE BRACE?
The FDA product code for ULNAR FRACTURE BRACE is IQI.
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 Orthomedics 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: IQI)
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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