INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301
K-Number: K072113 · 2007-10-10
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Device Summary
Frequently Asked Questions
What is the INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301?
INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301 is a medical device that received FDA 510(k) clearance on 2007-10-10. The listed applicant is Integra Lifesciences Corp.. The 510(k) number is K072113.
When did INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301 receive FDA 510(k) clearance?
INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301 received FDA 510(k) clearance on 2007-10-10, under 510(k) number K072113.
Who is the listed applicant for INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301?
The FDA 510(k) record lists Integra Lifesciences Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301?
The FDA product code for INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301 is KGN.
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 Integra Lifesciences Corp. 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: KGN)
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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