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FDA 510(k)

BONE GRAFT SYRINGE, MODEL 8600-00X0

K-Number: K023088 · 2002-10-02

ApplicantWrightmedicaltechnologyinc
Decision Date2002-10-02
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BONE GRAFT SYRINGE, MODEL 8600-00X0 is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2002-10-02 under 510(k) number K023088. 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 BONE GRAFT SYRINGE, MODEL 8600-00X0?

BONE GRAFT SYRINGE, MODEL 8600-00X0 is a medical device that received FDA 510(k) clearance on 2002-10-02. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K023088.

When did BONE GRAFT SYRINGE, MODEL 8600-00X0 receive FDA 510(k) clearance?

BONE GRAFT SYRINGE, MODEL 8600-00X0 received FDA 510(k) clearance on 2002-10-02, under 510(k) number K023088.

Who is the listed applicant for BONE GRAFT SYRINGE, MODEL 8600-00X0?

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

What is the FDA product code for BONE GRAFT SYRINGE, MODEL 8600-00X0?

The FDA product code for BONE GRAFT SYRINGE, MODEL 8600-00X0 is 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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