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FDA 510(k)

PCCS GRAFT DELIVERY SYSTEM

K-Number: K021071 · 2002-07-01

ApplicantBiomet, Inc.
Decision Date2002-07-01
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PCCS GRAFT DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2002-07-01 under 510(k) number K021071. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PCCS GRAFT DELIVERY SYSTEM?

PCCS GRAFT DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-01. The listed applicant is Biomet, Inc.. The 510(k) number is K021071.

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

PCCS GRAFT DELIVERY SYSTEM received FDA 510(k) clearance on 2002-07-01, under 510(k) number K021071.

Who is the listed applicant for PCCS GRAFT DELIVERY SYSTEM?

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

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

The FDA product code for PCCS GRAFT DELIVERY SYSTEM is FMF.

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Related Devices (Code: FMF)

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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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