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FDA 510(k)

SYMPHONY GRAFT DELIVERY SYSTEM

K-Number: K003286 · 2001-01-18

ApplicantDepuyacromed
Decision Date2001-01-18
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYMPHONY GRAFT DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuyacromed. It received FDA 510(k) clearance on 2001-01-18 under 510(k) number K003286. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMPHONY GRAFT DELIVERY SYSTEM?

SYMPHONY GRAFT DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2001-01-18. The listed applicant is Depuyacromed. The 510(k) number is K003286.

When did SYMPHONY GRAFT DELIVERY SYSTEM receive FDA 510(k) clearance?

SYMPHONY GRAFT DELIVERY SYSTEM received FDA 510(k) clearance on 2001-01-18, under 510(k) number K003286.

Who is the listed applicant for SYMPHONY GRAFT DELIVERY SYSTEM?

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

What is the FDA product code for SYMPHONY GRAFT DELIVERY SYSTEM?

The FDA product code for SYMPHONY GRAFT DELIVERY SYSTEM is LYC.

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Other records listing Depuyacromed as applicant

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Related Devices (Code: LYC)

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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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