Cleared Traditional

K864892 - ELLISON ARTHROSCOPY CHEATER

K864892 is an FDA 510(k) clearance for ELLISON ARTHROSCOPY CHEATER, manufactured by Buckman Co., Inc.. The device is a Class 2 Orthopedic device with product code HRX cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K864892 · Buckman Co., Inc. · Orthopedic device
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Dec 1986
Decision
15d
Days
Class 2
Risk

K864892 is an FDA 510(k) clearance for the ELLISON ARTHROSCOPY CHEATER. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Buckman Co., Inc. (Martinez, US). The FDA issued a Cleared decision on December 30, 1986 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.1100 - 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 Buckman Co., Inc. devices

FDA 510(k) Submission Details - K864892

510(k) Number K864892 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1986
Decision Date December 30, 1986
Days to Decision 15 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
107d faster than avg
Panel avg: 122d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HRX Device Classification - Class 2, Special Controls

Product Code HRX Arthroscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.1100
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HRX Arthroscope

All 547
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K864892.
THE KARL STORZ MODEL 28805 ARTHRO PUMP
K871621 · KARL STORZ Endoscopy-America, Inc. · Jun 1987
EFER ARTHROSCOPE
K870654 · Roseburg SA · May 1987
SIMPULSE ARTHROSCOPY IRRIGATION SYSTEM
K870915 · C.R. Bard, Inc. · Apr 1987
ARTHROSCOPIC SHOULDER LIGAMENT REPAIR KIT
K862017 · Dyonics, Inc. · Dec 1986
XENON LIGHT SOURCE FOR ENDOSCOPIC PROCEDURES
K863986 · American Edwards Laboratories · Oct 1986
CANCELLOUS SCREW
K862990 · Orthopedic Systems, Inc. · Oct 1986