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FDA 510(k)

XYLOS MACRO-POROUS SURGICAL MESH

K-Number: K111584 · 2011-08-25

ApplicantXylos Corporation
Decision Date2011-08-25
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

XYLOS MACRO-POROUS SURGICAL MESH is the device name listed in this FDA 510(k) record. The listed applicant is Xylos Corporation. It received FDA 510(k) clearance on 2011-08-25 under 510(k) number K111584. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XYLOS MACRO-POROUS SURGICAL MESH?

XYLOS MACRO-POROUS SURGICAL MESH is a medical device that received FDA 510(k) clearance on 2011-08-25. The listed applicant is Xylos Corporation. The 510(k) number is K111584.

When did XYLOS MACRO-POROUS SURGICAL MESH receive FDA 510(k) clearance?

XYLOS MACRO-POROUS SURGICAL MESH received FDA 510(k) clearance on 2011-08-25, under 510(k) number K111584.

Who is the listed applicant for XYLOS MACRO-POROUS SURGICAL MESH?

The FDA 510(k) record lists Xylos Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XYLOS MACRO-POROUS SURGICAL MESH?

The FDA product code for XYLOS MACRO-POROUS SURGICAL MESH is FTM.

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Other records listing Xylos Corporation 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.

K100984XYLOS VESSEL GUARDK090880XYLOS POROUS SURGICAL MESHK090778MTA PROTECTIVE SHEETK083823SECURIAN TISSUE REINFORCEMENT MATRIXK081882MODIFICATION TO XYLOS SURGICAL MESHK023237XYLOS SURGICAL MESH

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Related Devices (Code: FTM)

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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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