Cleared Traditional

K150259 - CLIP PLUS Disposable Clip Applier

Also marketed or referenced as:
CLIP PLUS Disposable Clip Applier,L

K150259 is an FDA 510(k) clearance for CLIP PLUS Disposable Clip Applier, manufactured by Taiwan Surgical Corporation. The device is a Class 2 General & Plastic Surgery device with product code FZP cleared through the Traditional 510(k) pathway after a 276-day FDA review.

K150259 · Taiwan Surgical Corporation · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2015
Decision
276d
Days
Class 2
Risk

K150259 is an FDA 510(k) clearance for the CLIP PLUS Disposable Clip Applier,ML. Classified as Clip, Implantable (product code FZP), Class II - Special Controls.

Submitted by Taiwan Surgical Corporation (Zhubei City, TW). The FDA issued a Cleared decision on November 6, 2015 after a review of 276 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4300 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Taiwan Surgical Corporation devices

FDA 510(k) Submission Details - K150259

510(k) Number K150259 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 2015
Decision Date November 06, 2015
Days to Decision 276 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
161d slower than avg
Panel avg: 115d · This submission: 276d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FZP Device Classification - Class 2, Special Controls

Product Code FZP Clip, Implantable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4300
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - FZP Clip, Implantable

All 105
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