MOSS - ANCHOR SET
K-Number: K913701 · 1992-02-14
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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 1992-02-14. The listed applicant is Moss Medical Products. The 510(k) number is K913701.
When did MOSS - ANCHOR SET receive FDA 510(k) clearance?
MOSS - ANCHOR SET received FDA 510(k) clearance on 1992-02-14, under 510(k) number K913701.
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 FPD.
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: FPD)
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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