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FDA 510(k)

MICRO DYNAMIC MESH

K-Number: K983528 · 1998-12-23

ApplicantHowmedica Corp.
Decision Date1998-12-23
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO DYNAMIC MESH is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1998-12-23 under 510(k) number K983528. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO DYNAMIC MESH?

MICRO DYNAMIC MESH is a medical device that received FDA 510(k) clearance on 1998-12-23. The listed applicant is Howmedica Corp.. The 510(k) number is K983528.

When did MICRO DYNAMIC MESH receive FDA 510(k) clearance?

MICRO DYNAMIC MESH received FDA 510(k) clearance on 1998-12-23, under 510(k) number K983528.

Who is the listed applicant for MICRO DYNAMIC MESH?

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

What is the FDA product code for MICRO DYNAMIC MESH?

The FDA product code for MICRO DYNAMIC MESH is JEY.

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Other records listing Howmedica Corp. as applicant

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Related Devices (Code: JEY)

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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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