FDA 510(k)

SNIPER STAPLE SYSTEM, NON-STERILE

K-Number: K172405 · 2017-12-11

Decision Date2017-12-11

Product CodeJDR

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SNIPER STAPLE SYSTEM, NON-STERILE is a medical device manufactured by Trilliant Surgical. It received FDA 510(k) clearance on 2017-12-11 under approval number K172405. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNIPER STAPLE SYSTEM, NON-STERILE?

SNIPER STAPLE SYSTEM, NON-STERILE is a medical device that received FDA 510(k) clearance on 2017-12-11. It is manufactured by Trilliant Surgical. The 510(k) number is K172405.

When was SNIPER STAPLE SYSTEM, NON-STERILE approved by the FDA?

SNIPER STAPLE SYSTEM, NON-STERILE received FDA 510(k) clearance on 2017-12-11, under approval number K172405.

What company makes SNIPER STAPLE SYSTEM, NON-STERILE?

SNIPER STAPLE SYSTEM, NON-STERILE is manufactured by Trilliant Surgical.

What is the FDA product code for SNIPER STAPLE SYSTEM, NON-STERILE?

The FDA product code for SNIPER STAPLE SYSTEM, NON-STERILE is JDR.

Other Devices by Trilliant Surgical

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.