Cleared Traditional

K935592 - SURGICAL ACCESSORIES COCR CABLE SYSTEM

K935592 is an FDA 510(k) clearance for SURGICAL ACCESSORIES COCR CABLE SYSTEM, manufactured by Surgical Accessories, Inc.. The device is a Class 2 Orthopedic device with product code JDQ cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K935592 · Surgical Accessories, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1994
Decision
68d
Days
Class 2
Risk

K935592 is an FDA 510(k) clearance for the SURGICAL ACCESSORIES COCR CABLE SYSTEM. Classified as Cerclage, Fixation (product code JDQ), Class II - Special Controls.

Submitted by Surgical Accessories, Inc. (St. Louis, US). The FDA issued a Cleared decision on January 26, 1994 after a review of 68 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3010 - 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 Surgical Accessories, Inc. devices

FDA 510(k) Submission Details - K935592

510(k) Number K935592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 19, 1993
Decision Date January 26, 1994
Days to Decision 68 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
54d faster than avg
Panel avg: 122d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDQ Device Classification - Class 2, Special Controls

Product Code JDQ Cerclage, Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3010
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 - JDQ Cerclage, Fixation

All 120
Devices cleared under the same product code (JDQ) and FDA review panel - the closest regulatory comparables to K935592.
DALL MILES SYSTEM MINICLEAT
K934058 · Howmedica Corp. · Feb 1994
CERCLAGE WIRE CRIMP SLEEVE
K931246 · Acu Med, Inc. · Feb 1994
SPONGER CABLE SYSTEM, MODIFICATION
K935481 · Pioneer Surgical Technology · Jan 1994
ORTHOPAEDIC POLYETHYLENE CABLE
K924141 · Smith & Nephew Richards, Inc. · Nov 1993
OTI ORTHOPEDIC WIRE SYSTEM
K925447 · Osteo Technology, Inc. · Jun 1993
STERNAL BAND
K930015 · Stony Brook Surgical Innovations, Inc. · May 1993