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FDA 510(k)

SMF RESORBABLE MESHES AND SHEETS

K-Number: K003786 · 2001-02-27

ApplicantSynthes (Usa)
Decision Date2001-02-27
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SMF RESORBABLE MESHES AND SHEETS is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2001-02-27 under 510(k) number K003786. 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 SMF RESORBABLE MESHES AND SHEETS?

SMF RESORBABLE MESHES AND SHEETS is a medical device that received FDA 510(k) clearance on 2001-02-27. The listed applicant is Synthes (Usa). The 510(k) number is K003786.

When did SMF RESORBABLE MESHES AND SHEETS receive FDA 510(k) clearance?

SMF RESORBABLE MESHES AND SHEETS received FDA 510(k) clearance on 2001-02-27, under 510(k) number K003786.

Who is the listed applicant for SMF RESORBABLE MESHES AND SHEETS?

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

What is the FDA product code for SMF RESORBABLE MESHES AND SHEETS?

The FDA product code for SMF RESORBABLE MESHES AND SHEETS is JEY.

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 Synthes (Usa) 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.

View all 409 devices →

Related Devices (Code: JEY)

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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