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FDA 510(k)

MODIFICATION TO BONE GRAFT SYRINGE

K-Number: K062173 · 2006-08-23

ApplicantWrightmedicaltechnologyinc
Decision Date2006-08-23
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO BONE GRAFT SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2006-08-23 under 510(k) number K062173. 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 MODIFICATION TO BONE GRAFT SYRINGE?

MODIFICATION TO BONE GRAFT SYRINGE is a medical device that received FDA 510(k) clearance on 2006-08-23. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K062173.

When did MODIFICATION TO BONE GRAFT SYRINGE receive FDA 510(k) clearance?

MODIFICATION TO BONE GRAFT SYRINGE received FDA 510(k) clearance on 2006-08-23, under 510(k) number K062173.

Who is the listed applicant for MODIFICATION TO BONE GRAFT SYRINGE?

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 MODIFICATION TO BONE GRAFT SYRINGE?

The FDA product code for MODIFICATION TO BONE GRAFT SYRINGE 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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