Cleared Traditional

K926303 - ARTHREX INSTRUMENTS (WRIST)

K926303 is the FDA 510(k) clearance for ARTHREX INSTRUMENTS (WRIST) by Arthrex, Inc.. It is a Class 2 Orthopedic device (product code HRX) cleared through the Traditional 510(k) pathway after a 407-day FDA review.

K926303 · Arthrex, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1994
Decision
407d
Days
Class 2
Risk

K926303 is an FDA 510(k) clearance for the ARTHREX INSTRUMENTS (WRIST). Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on January 26, 1994 after a review of 407 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

View all Arthrex, Inc. devices

Submission Details

510(k) Number K926303 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1992
Decision Date January 26, 1994
Days to Decision 407 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
285d slower than avg
Panel avg: 122d · This submission: 407d
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 376
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K926303.
ARTHREX TIBIAL TUNNEL CANNULA
K930152 · Arthrex, Inc. · Mar 1994
ACUFEX ARTHROSCOPE
K934270 · Acufex Microsurgical, Inc. · Feb 1994
ARTHREX INSTRUMENTS ( HIP )
K926212 · Arthrex, Inc. · Jan 1994
ACUFEX PRO-PAC AND ISO-PAC
K931621 · Acufex Microsurgical, Inc. · Jan 1994
SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.
K924016 · Symbiosis Corp. · Dec 1993
RESTORE TUNNEL PLUG
K923069 · Depuy, Inc. · Jun 1993