Cleared Traditional

K822561 - MICROSCOPE

K822561 is the FDA 510(k) clearance for MICROSCOPE by Treace Medical, Inc.. It is a Class 1 General & Plastic Surgery device (product code EPT) cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K822561 · Treace Medical, Inc. · General & Plastic Surgery device
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Sep 1982
Decision
21d
Days
Class 1
Risk

K822561 is an FDA 510(k) clearance for the MICROSCOPE. Classified as Microscope, Surgical (product code EPT), Class I - General Controls.

Submitted by Treace Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 14, 1982 after a review of 21 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4700 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Treace Medical, Inc. devices

Submission Details

510(k) Number K822561 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 24, 1982
Decision Date September 14, 1982
Days to Decision 21 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 115d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EPT Microscope, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4700
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 - EPT Microscope, Surgical

All 12
Devices cleared under the same product code (EPT) and FDA review panel - the closest regulatory comparables to K822561.
STORZ DIAGNOSTIC MICROSCOPE SYSTEM
K882269 · Storz Instrument Co. · Jun 1988
ZEISS VOICE CONTROL SYSTEM FOR OPMI'S
K860811 · Carl Zeiss, Inc. · Apr 1986
STORZ/URBAN SURGICAL MICROSCOPE SYSTEM
K844858 · Storz Instrument Co. · Mar 1985
NAGASHIMA SU-A CEILING MOUNT UNIT FOR
K822014 · Kelleher Corp. · Aug 1982
BINOCULAR OPERATING MICROSCOPES &
K822009 · Kelleher Corp. · Jul 1982
STORZ/OLYMPUS MICROSCOPE SYSTEM
K812234 · Storz Instrument Co. · Sep 1981