MOSS- ANCHOR SET
K-Number: K910910 · 1991-06-24
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Device Summary
Frequently Asked Questions
What is the MOSS- ANCHOR SET?
MOSS- ANCHOR SET is a medical device that received FDA 510(k) clearance on 1991-06-24. The listed applicant is Moss Medical Products. The 510(k) number is K910910.
When did MOSS- ANCHOR SET receive FDA 510(k) clearance?
MOSS- ANCHOR SET received FDA 510(k) clearance on 1991-06-24, under 510(k) number K910910.
Who is the listed applicant for MOSS- ANCHOR SET?
The FDA 510(k) record lists Moss Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOSS- ANCHOR SET?
The FDA product code for MOSS- ANCHOR SET is KNT.
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 Moss Medical 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: KNT)
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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