SURGIMESH XB - SKIRTED
K-Number: K120025 · 2012-06-26
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Device Summary
Frequently Asked Questions
What is the SURGIMESH XB - SKIRTED?
SURGIMESH XB - SKIRTED is a medical device that received FDA 510(k) clearance on 2012-06-26. The listed applicant is Aspide Medical. The 510(k) number is K120025.
When did SURGIMESH XB - SKIRTED receive FDA 510(k) clearance?
SURGIMESH XB - SKIRTED received FDA 510(k) clearance on 2012-06-26, under 510(k) number K120025.
Who is the listed applicant for SURGIMESH XB - SKIRTED?
The FDA 510(k) record lists Aspide Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIMESH XB - SKIRTED?
The FDA product code for SURGIMESH XB - SKIRTED is FTL.
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 Aspide Medical 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: FTL)
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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