G-FLOSS & G-FLOSS II
K-Number: K911701 · 1991-05-15
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Device Summary
Frequently Asked Questions
What is the G-FLOSS & G-FLOSS II?
G-FLOSS & G-FLOSS II is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K911701.
When did G-FLOSS & G-FLOSS II receive FDA 510(k) clearance?
G-FLOSS & G-FLOSS II received FDA 510(k) clearance on 1991-05-15, under 510(k) number K911701.
Who is the listed applicant for G-FLOSS & G-FLOSS II?
The FDA 510(k) record lists Implant Innovations International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-FLOSS & G-FLOSS II?
The FDA product code for G-FLOSS & G-FLOSS II is JES.
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 Implant Innovations International, Inc. 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: JES)
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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