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FDA 510(k)

BONESOURCE HAC

K-Number: K021440 · 2002-08-02

ApplicantStryker Instruments
Decision Date2002-08-02
Product CodeGXP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BONESOURCE HAC is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2002-08-02 under 510(k) number K021440. The device is classified under product code GXP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONESOURCE HAC?

BONESOURCE HAC is a medical device that received FDA 510(k) clearance on 2002-08-02. The listed applicant is Stryker Instruments. The 510(k) number is K021440.

When did BONESOURCE HAC receive FDA 510(k) clearance?

BONESOURCE HAC received FDA 510(k) clearance on 2002-08-02, under 510(k) number K021440.

Who is the listed applicant for BONESOURCE HAC?

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

What is the FDA product code for BONESOURCE HAC?

The FDA product code for BONESOURCE HAC is GXP.

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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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