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FDA 510(k)

FSSB NYLON SURGICAL SUTURES

K-Number: K060471 · 2006-07-26

Decision Date2006-07-26
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FSSB NYLON SURGICAL SUTURES is the device name listed in this FDA 510(k) record. The listed applicant is Fssb Chirurgische Nadeln GmbH. It received FDA 510(k) clearance on 2006-07-26 under 510(k) number K060471. The device is classified under product code GAR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FSSB NYLON SURGICAL SUTURES?

FSSB NYLON SURGICAL SUTURES is a medical device that received FDA 510(k) clearance on 2006-07-26. The listed applicant is Fssb Chirurgische Nadeln GmbH. The 510(k) number is K060471.

When did FSSB NYLON SURGICAL SUTURES receive FDA 510(k) clearance?

FSSB NYLON SURGICAL SUTURES received FDA 510(k) clearance on 2006-07-26, under 510(k) number K060471.

Who is the listed applicant for FSSB NYLON SURGICAL SUTURES?

The FDA 510(k) record lists Fssb Chirurgische Nadeln GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FSSB NYLON SURGICAL SUTURES?

The FDA product code for FSSB NYLON SURGICAL SUTURES is GAR.

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.

Related Devices (Code: GAR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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