MITEK QUICKANCHOR(TM), MODIFICATION
K-Number: K915089 · 1992-02-03
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Device Summary
Frequently Asked Questions
What is the MITEK QUICKANCHOR(TM), MODIFICATION?
MITEK QUICKANCHOR(TM), MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Mitek Surgical Products, Inc.. The 510(k) number is K915089.
When did MITEK QUICKANCHOR(TM), MODIFICATION receive FDA 510(k) clearance?
MITEK QUICKANCHOR(TM), MODIFICATION received FDA 510(k) clearance on 1992-02-03, under 510(k) number K915089.
Who is the listed applicant for MITEK QUICKANCHOR(TM), MODIFICATION?
The FDA 510(k) record lists Mitek Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MITEK QUICKANCHOR(TM), MODIFICATION?
The FDA product code for MITEK QUICKANCHOR(TM), MODIFICATION is GAS.
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 Mitek Surgical Products, 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: GAS)
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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