Cleared Traditional

InnoClip Disposable Clip Applier, InnoClip Clip Applier

K202994 · Taiwan Surgical Corporation · General & Plastic Surgery
Jan 2022
Decision
460d
Days
Class 2
Risk

About This 510(k) Submission

K202994 is an FDA 510(k) clearance for the InnoClip Disposable Clip Applier, InnoClip Clip Applier, a Clip, Implantable (Class II — Special Controls, product code FZP), submitted by Taiwan Surgical Corporation (Zhubei City, TW). The FDA issued a Cleared decision on January 4, 2022, 460 days after receiving the submission on October 1, 2020. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4300.

Submission Details

510(k) Number K202994 FDA.gov
FDA Decision Cleared SESE
Date Received October 01, 2020
Decision Date January 04, 2022
Days to Decision 460 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FZP — Clip, Implantable
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4300

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