KNEE SEPARATOR
K-Number: K770167 · 1977-01-28
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Device Summary
Frequently Asked Questions
What is the KNEE SEPARATOR?
KNEE SEPARATOR is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Bel-Art Products. The 510(k) number is K770167.
When did KNEE SEPARATOR receive FDA 510(k) clearance?
KNEE SEPARATOR received FDA 510(k) clearance on 1977-01-28, under 510(k) number K770167.
Who is the listed applicant for KNEE SEPARATOR?
The FDA 510(k) record lists Bel-Art Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KNEE SEPARATOR?
The FDA product code for KNEE SEPARATOR 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 Bel-Art Products 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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