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FDA 510(k)

SNIPER STAPLE SYSTEM, NON-STERILE

K-Number: K172405 · 2017-12-11

ApplicantTrilliant Surgical
Decision Date2017-12-11
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SNIPER STAPLE SYSTEM, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Trilliant Surgical. It received FDA 510(k) clearance on 2017-12-11 under 510(k) 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. The listed applicant is Trilliant Surgical. The 510(k) number is K172405.

When did SNIPER STAPLE SYSTEM, NON-STERILE receive FDA 510(k) clearance?

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

Who is the listed applicant for SNIPER STAPLE SYSTEM, NON-STERILE?

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

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 records listing Trilliant Surgical as applicant

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Related Devices (Code: JDR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261121Megalodon Dynamic Compression SystemParagon 28, Inc.K250712Linkt Compression Staple SystemTrax SurgicalK243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LPK243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.K243658TMC Compression Implant SystemTreace Medical ConceptsK242415TMC Compression Implant SystemTreace Medical Concepts

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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