Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MOSS - ANCHOR SET

K-Number: K913701 · 1992-02-14

Decision Date1992-02-14
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOSS - ANCHOR SET is the device name listed in this FDA 510(k) record. The listed applicant is Moss Medical Products. It received FDA 510(k) clearance on 1992-02-14 under 510(k) number K913701. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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.

↑