Cleared Traditional

K862933 - ABC-1000 SMALL JOINT REAMERS

K862933 is the FDA 510(k) clearance for ABC-1000 SMALL JOINT REAMERS by Instrumentation Industries, Inc.. It is a Class 1 Orthopedic device (product code HTO) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K862933 · Instrumentation Industries, Inc. · Orthopedic device
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Aug 1986
Decision
14d
Days
Class 1
Risk

K862933 is an FDA 510(k) clearance for the ABC-1000 SMALL JOINT REAMERS. Classified as Reamer (product code HTO), Class I - General Controls.

Submitted by Instrumentation Industries, Inc. (Bethel Park, US). The FDA issued a Cleared decision on August 18, 1986 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.4540 - the FDA orthopedic device regulatory 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 Instrumentation Industries, Inc. devices

Submission Details

510(k) Number K862933 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1986
Decision Date August 18, 1986
Days to Decision 14 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
108d faster than avg
Panel avg: 122d · This submission: 14d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HTO Reamer
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.4540
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 - HTO Reamer

All 10
Devices cleared under the same product code (HTO) and FDA review panel - the closest regulatory comparables to K862933.
SYNTHES REAMER/IRRIGATOR/ASPIRATOR (RIA) SYSTEM
K993335 · Synthes (Usa) · Jun 2000
FLEXIBLE INTRAMEDULLARY REAMER
K954915 · Zimmer, Inc. · Dec 1995
COMBINATION REAMER
K903248 · Onyx Medical Corp. · Jul 1990
MEDULLARY CANAL SCRAPERS
K811081 · The Anspach Effort, Inc. · Apr 1981
C.C.F. FEMORAL DEBRIDEMENT PROBE
K790996 · Depuy, Inc. · Jun 1979
FLEXIBLE REAMER, GUIDE WIRE SYSTEM
K790307 · 3M Company · Feb 1979