Cleared Traditional

DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION (K934299) - FDA 510(k) Clearance

Class II Orthopedic device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K934299 · Smith & Nephew Dyonics, Inc. · Orthopedic device
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Feb 1994
Decision
165d
Days
Class 2
Risk

K934299 is an FDA 510(k) clearance for the DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Smith & Nephew Dyonics, Inc. (Andover, US). The FDA issued a Cleared decision on February 14, 1994 after a review of 165 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Smith & Nephew Dyonics, Inc. devices

Submission Details

510(k) Number K934299 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 02, 1993
Decision Date February 14, 1994
Days to Decision 165 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d slower than avg
Panel avg: 122d · This submission: 165d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 178
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K934299.
GORE SMOOTHER CRUCIAL TOOL
K936206 · W.L. Gore & Associates, Inc. · Mar 1994
DISPOSABLE ARTHROSCOPIC ACCESSORY
K933949 · United States Surgical, A Division of Tyco Healthc · Mar 1994
ARTHREX TIBIAL TUNNEL CANNULA
K930152 · Arthrex, Inc. · Mar 1994
ARTHREX INSTRUMENTS ( HIP )
K926212 · Arthrex, Inc. · Jan 1994
ARTHREX INSTRUMENTS (WRIST)
K926303 · Arthrex, Inc. · Jan 1994
RESTORE TUNNEL PLUG
K923069 · Depuy, Inc. · Jun 1993