FDA 510(k)

V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE

K-Number: K103052 · 2010-11-10

Decision Date2010-11-10

Product CodeGAT

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Covidien, LLC. It received FDA 510(k) clearance on 2010-11-10 under 510(k) number K103052. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE?

V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE is a medical device that received FDA 510(k) clearance on 2010-11-10. The listed applicant is Covidien, LLC. The 510(k) number is K103052.

When did V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE receive FDA 510(k) clearance?

V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE received FDA 510(k) clearance on 2010-11-10, under 510(k) number K103052.

Who is the listed applicant for V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE?

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

What is the FDA product code for V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE?

The FDA product code for V-LOC(TM) NONABSORBABLE WOUND CLOSURE DEVICE is GAT.

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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.