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FDA 510(k)

MEDTRONIC GRAFT DELIVERY SYRINGE

K-Number: K062986 · 2006-12-08

ApplicantMedtronic Sofamor Danek USA, Inc.
Decision Date2006-12-08
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC GRAFT DELIVERY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek USA, Inc.. It received FDA 510(k) clearance on 2006-12-08 under 510(k) number K062986. 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 MEDTRONIC GRAFT DELIVERY SYRINGE?

MEDTRONIC GRAFT DELIVERY SYRINGE is a medical device that received FDA 510(k) clearance on 2006-12-08. The listed applicant is Medtronic Sofamor Danek USA, Inc.. The 510(k) number is K062986.

When did MEDTRONIC GRAFT DELIVERY SYRINGE receive FDA 510(k) clearance?

MEDTRONIC GRAFT DELIVERY SYRINGE received FDA 510(k) clearance on 2006-12-08, under 510(k) number K062986.

Who is the listed applicant for MEDTRONIC GRAFT DELIVERY SYRINGE?

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

What is the FDA product code for MEDTRONIC GRAFT DELIVERY SYRINGE?

The FDA product code for MEDTRONIC GRAFT DELIVERY SYRINGE 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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