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FDA 510(k)

SUPRAMID EXTRA SURGICAL MESH

K-Number: K831723 · 1983-08-12

ApplicantS. Jackson, Inc.
Decision Date1983-08-12
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUPRAMID EXTRA SURGICAL MESH is the device name listed in this FDA 510(k) record. The listed applicant is S. Jackson, Inc.. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K831723. 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 SUPRAMID EXTRA SURGICAL MESH?

SUPRAMID EXTRA SURGICAL MESH is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is S. Jackson, Inc.. The 510(k) number is K831723.

When did SUPRAMID EXTRA SURGICAL MESH receive FDA 510(k) clearance?

SUPRAMID EXTRA SURGICAL MESH received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831723.

Who is the listed applicant for SUPRAMID EXTRA SURGICAL MESH?

The FDA 510(k) record lists S. Jackson, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPRAMID EXTRA SURGICAL MESH?

The FDA product code for SUPRAMID EXTRA SURGICAL MESH is FTM.

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Other records listing S. Jackson, 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.

K080216SUPRAMESH EXTRAK973379STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETSK931613SUPRAMID SUTUREK931612NYLAMID SUTUREK931614MOPYLEN SUTUREK922630MOPYLEN

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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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