Cleared Traditional

K010184 - CHESS HAND SURGERY SYSTEM

K010184 is an FDA 510(k) clearance for CHESS HAND SURGERY SYSTEM, manufactured by Canica Design, Inc.. The device is a Class 1 General & Plastic Surgery device with product code MDM cleared through the Traditional 510(k) pathway after a 154-day FDA review.

K010184 · Canica Design, Inc. · General & Plastic Surgery device
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Jun 2001
Decision
154d
Days
Class 1
Risk

K010184 is an FDA 510(k) clearance for the CHESS HAND SURGERY SYSTEM. Classified as Instrument, Manual, Surgical, General Use (product code MDM), Class I - General Controls.

Submitted by Canica Design, Inc. (Almonte, Ontario, CA). The FDA issued a Cleared decision on June 22, 2001 after a review of 154 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 Canica Design, Inc. devices

FDA 510(k) Submission Details - K010184

510(k) Number K010184 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 19, 2001
Decision Date June 22, 2001
Days to Decision 154 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d slower than avg
Panel avg: 115d · This submission: 154d
Pathway characteristics
Predicate-based equivalence.

MDM Device Classification - Class 1, General Controls

Product Code MDM Instrument, Manual, Surgical, General Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - MDM Instrument, Manual, Surgical, General Use

All 11
Devices cleared under the same product code (MDM) and FDA review panel - the closest regulatory comparables to K010184.
MICROVASIVE PULMONARY GUIDEWIRE
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K981579 · Ethicon, Inc. · Jul 1998
CLAMPS AND CLIPS
K942896 · Surgin Surgical Instrumentation, Inc. · Jul 1994
ORC ENDOSCOPIC INSTRUMENT HOLDER
K930399 · O.R. Concepts, Inc. · Feb 1993
LACERATION REPAIR TRAY
K921988 · Cypress Medical Products, Ltd. · Nov 1992