Cleared Traditional

K802503 - MICRO-SUGICAL POWER INSTRUMENT SYSTEM

K802503 is an FDA 510(k) clearance for MICRO-SUGICAL POWER INSTRUMENT SYSTEM, manufactured by Spire Medical, Inc.. The device is a Class 1 Ear, Nose, Throat device with product code EQJ cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K802503 · Spire Medical, Inc. · Ear, Nose, Throat device
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Oct 1980
Decision
14d
Days
Class 1
Risk

K802503 is an FDA 510(k) clearance for the MICRO-SUGICAL POWER INSTRUMENT SYSTEM. Classified as Bur, Ear, Nose And Throat (product code EQJ), Class I - General Controls.

Submitted by Spire Medical, Inc. (Ventura, US). The FDA issued a Cleared decision on October 31, 1980 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.4140 - the FDA ear, nose and throat 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 Spire Medical, Inc. devices

FDA 510(k) Submission Details - K802503

510(k) Number K802503 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 17, 1980
Decision Date October 31, 1980
Days to Decision 14 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 89d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

EQJ Device Classification - Class 1, General Controls

Product Code EQJ Bur, Ear, Nose And Throat
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.4140
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 - EQJ Bur, Ear, Nose And Throat

All 10
Devices cleared under the same product code (EQJ) and FDA review panel - the closest regulatory comparables to K802503.
ESSENTIAL SHAVER SYSTEM
K953096 · Smith & Nephew Richards, Inc. · Jul 1995
KARL STORZ MICRO-INSTRUMENT FOR COCHLEAR IMPLANTATION
K946332 · KARL STORZ Endoscopy-America, Inc. · Jun 1995
MICROMEDICS EAR, NOSE AND THROAT BURS
K895738 · Micromedics, Inc. · Dec 1989
OTOTOME BUR
K792028 · American Sterilizer Co. · Oct 1979