Cleared Traditional

K863988 - THORTON TITANIUM HOOK ANGLED RIGHT

K863988 is the FDA 510(k) clearance for THORTON TITANIUM HOOK ANGLED RIGHT by Keeler Instruments, Inc.. It is a Class 1 Ophthalmic device (product code HNQ) cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K863988 · Keeler Instruments, Inc. · Ophthalmic device
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Oct 1986
Decision
17d
Days
Class 1
Risk

K863988 is an FDA 510(k) clearance for the THORTON TITANIUM HOOK ANGLED RIGHT. Classified as Hook, Ophthalmic (product code HNQ), Class I - General Controls.

Submitted by Keeler Instruments, Inc. (Broomall, US). The FDA issued a Cleared decision on October 31, 1986 after a review of 17 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 Keeler Instruments, Inc. devices

Submission Details

510(k) Number K863988 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 1986
Decision Date October 31, 1986
Days to Decision 17 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 110d · This submission: 17d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HNQ Hook, 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 - HNQ Hook, Ophthalmic

Devices cleared under the same product code (HNQ) and FDA review panel - the closest regulatory comparables to K863988.
PRISMA DISPOSABLE IRRIGATING IRIS HOOK
K874991 · Advanced Surgical Products, Inc. · Apr 1988
BONN MICRO IRIS HOOK (NON-STERILE) #7613
K801469 · Edward Weck, Inc. · Jul 1980
HOOKS #'S 7600,7602,7603,7616
K791985 · Edward Weck, Inc. · Oct 1979
HOOK, IRIS, SHEPARD U-SHAPED
K770103 · Edward Weck, Inc. · Jan 1977
HOOK, IRIS, HERSHMAN
K770098 · Edward Weck, Inc. · Jan 1977