FDA 510(k)

MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)

K-Number: K972906 · 1998-02-06

Decision Date1998-02-06

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1998-02-06 under 510(k) number K972906. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)?

MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA) is a medical device that received FDA 510(k) clearance on 1998-02-06. The listed applicant is Medtronic Vascular. The 510(k) number is K972906.

When did MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA) receive FDA 510(k) clearance?

MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA) received FDA 510(k) clearance on 1998-02-06, under 510(k) number K972906.

Who is the listed applicant for MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)?

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

What is the FDA product code for MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA)?

The FDA product code for MEDTRONIC TWIST LOCK ANCHOR (PARTNUMBER 103953/3550TLA) is GZB.

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Official Source

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