FDA 510(k)

SUPER SCISSORS

K-Number: K870763 · 1987-03-18

Decision Date1987-03-18

Product Code

DecisionSubstantially Equivalent

Device Summary

SUPER 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 1987-03-18 under 510(k) number K870763. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER SCISSORS?

SUPER SCISSORS is a medical device that received FDA 510(k) clearance on 1987-03-18. The listed applicant is Treace Medical, Inc.. The 510(k) number is K870763.

When did SUPER SCISSORS receive FDA 510(k) clearance?

SUPER SCISSORS received FDA 510(k) clearance on 1987-03-18, under 510(k) number K870763.

Who is the listed applicant for SUPER SCISSORS?

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

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Treace Medical, Inc. as applicant

K883727BUCKET PROSTHESIS PORP K882349MALLET, SURGICAL K874779BIPOLATOR 50 K873154TREACE MAGNUM OTO-TOOL SYSTEM K872000EYE GARD K870765CANNULATED INSTRUMENT CLEANERS

View all 80 devices →

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.