Cleared Traditional

K864520 - BARRON ROTARY BLADE TREPHINE USING HESS...

K864520 is the FDA 510(k) clearance for BARRON ROTARY BLADE TREPHINE USING HESS... by Precision Instruments, Inc.. It is a Class 1 Ophthalmic device (product code HRH) cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K864520 · Precision Instruments, Inc. · Ophthalmic device
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Jan 1987
Decision
64d
Days
Class 1
Risk

K864520 is an FDA 510(k) clearance for the BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON. Classified as Trephine, Manual, Ophthalmic (product code HRH), Class I - General Controls.

Submitted by Precision Instruments, Inc. (Grand Blanc, US). The FDA issued a Cleared decision on January 20, 1987 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4350 - the FDA ophthalmic 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 Precision Instruments, Inc. devices

Submission Details

510(k) Number K864520 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 1986
Decision Date January 20, 1987
Days to Decision 64 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 110d · This submission: 64d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HRH Trephine, Manual, Ophthalmic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4350
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 - HRH Trephine, Manual, Ophthalmic

Devices cleared under the same product code (HRH) and FDA review panel - the closest regulatory comparables to K864520.
DEKNATEL (R) TREPHINE
K862524 · Deknatel, Inc. · Aug 1986
CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADE
K861825 · Storz Instrument Co. · Jun 1986
PEARCE CORNEAL TREPHINE
K812723 · Visitec Co. · Oct 1981
CORNEAL CUTTER AND ACCESSORIES
K781411 · Codman & Shurtleff, Inc. · Sep 1978
TROUTMAN CORNEAL PUNCH
K771866 · Edward Weck, Inc. · Nov 1977