Cleared Traditional

K974579 - PERCSCOPE MODEL 2600

K974579 is an FDA 510(k) clearance for PERCSCOPE MODEL 2600, manufactured by Clarus Medical Systems, Inc.. The device is a Class 2 Orthopedic device with product code HRX cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K974579 · Clarus Medical Systems, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1998
Decision
72d
Days
Class 2
Risk

K974579 is an FDA 510(k) clearance for the PERCSCOPE MODEL 2600. Classified as Arthroscope (product code HRX), Class II - Special Controls.

Submitted by Clarus Medical Systems, Inc. (Minneapolis, US). The FDA issued a Cleared decision on February 18, 1998 after a review of 72 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 Clarus Medical Systems, Inc. devices

FDA 510(k) Submission Details - K974579

510(k) Number K974579 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1997
Decision Date February 18, 1998
Days to Decision 72 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 122d · This submission: 72d
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 394
Devices cleared under the same product code (HRX) and FDA review panel - the closest regulatory comparables to K974579.
UNIVERSAL DRIVE SYSTEM
K981269 · Linvatec Corp. · Jun 1998
DYONICS INTELIJET INFLOW/OUTFLOW CANNULA
K981156 · Smith & Nephew, Inc. · May 1998
YEUNG ENDOSCOPIC SPINE SYSTEM
K973405 · Richard Wolf Medical Instruments Corp. · Mar 1998
XPS STRAIGHTSHOT MICROBRIDER SYSTEM OR TREBAY SHAVER SYSTEM
K973499 · Xomed, Inc. · Jan 1998
KSEA ARTHROPUMP PLUS
K971649 · KARL STORZ Endoscopy-America, Inc. · Oct 1997
TOTAL PERFORMANCE SYSTEM SHAVER
K973195 · Stryker Endoscopy · Oct 1997