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FDA 510(k)

VEIN GRAFT EAR SCISSORS

K-Number: K870756 · 1987-03-03

ApplicantTreace Medical, Inc.
Decision Date1987-03-03
Product CodeJZB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VEIN GRAFT EAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1987-03-03 under 510(k) number K870756. The device is classified under product code JZB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEIN GRAFT EAR SCISSORS?

VEIN GRAFT EAR SCISSORS is a medical device that received FDA 510(k) clearance on 1987-03-03. The listed applicant is Treace Medical, Inc.. The 510(k) number is K870756.

When did VEIN GRAFT EAR SCISSORS receive FDA 510(k) clearance?

VEIN GRAFT EAR SCISSORS received FDA 510(k) clearance on 1987-03-03, under 510(k) number K870756.

Who is the listed applicant for VEIN GRAFT EAR SCISSORS?

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

What is the FDA product code for VEIN GRAFT EAR SCISSORS?

The FDA product code for VEIN GRAFT EAR SCISSORS is JZB.

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Other records listing Treace Medical, Inc. as applicant

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.

K883727BUCKET PROSTHESIS PORPK882349MALLET, SURGICALK874779BIPOLATOR 50K873154TREACE MAGNUM OTO-TOOL SYSTEMK872000EYE GARDK870765CANNULATED INSTRUMENT CLEANERS

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Related Devices (Code: JZB)

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.

K914226ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACKE.I. Dupont DE Nemours & Co., Inc.K833603SCISSORS SHEA BELLUCCMicrotek Medical, Inc.K822196EAR SCISSORSKelleher Corp.

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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