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FDA 510(k)

QUICKBRIDGE TM CYLINDER AND CAP

K-Number: K071551 · 2007-08-30

ApplicantBiomet 3i, Inc.
Decision Date2007-08-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

QUICKBRIDGE TM CYLINDER AND CAP is the device name listed in this FDA 510(k) record. The listed applicant is Biomet 3i, Inc.. It received FDA 510(k) clearance on 2007-08-30 under 510(k) number K071551. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKBRIDGE TM CYLINDER AND CAP?

QUICKBRIDGE TM CYLINDER AND CAP is a medical device that received FDA 510(k) clearance on 2007-08-30. The listed applicant is Biomet 3i, Inc.. The 510(k) number is K071551.

When did QUICKBRIDGE TM CYLINDER AND CAP receive FDA 510(k) clearance?

QUICKBRIDGE TM CYLINDER AND CAP received FDA 510(k) clearance on 2007-08-30, under 510(k) number K071551.

Who is the listed applicant for QUICKBRIDGE TM CYLINDER AND CAP?

The FDA 510(k) record lists Biomet 3i, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICKBRIDGE TM CYLINDER AND CAP?

The FDA product code for QUICKBRIDGE TM CYLINDER AND CAP is NHA.

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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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