Cleared Traditional

K964259 - SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION

K964259 is an FDA 510(k) clearance for SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION, manufactured by Synthes (Usa). The device is a Class 2 Orthopedic device with product code JDO cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K964259 · Synthes (Usa) · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1997
Decision
76d
Days
Class 2
Risk

K964259 is an FDA 510(k) clearance for the SYNTHES (USA) DDHS/DCS SYSTEM MODIFICATION. Classified as Device, Fixation, Proximal Femoral, Implant (product code JDO), Class II - Special Controls.

Submitted by Synthes (Usa) (Paoli, US). The FDA issued a Cleared decision on January 9, 1997 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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 Synthes (Usa) devices

FDA 510(k) Submission Details - K964259

510(k) Number K964259 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 1996
Decision Date January 09, 1997
Days to Decision 76 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 122d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDO Device Classification - Class 2, Special Controls

Product Code JDO Device, Fixation, Proximal Femoral, Implant
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 - JDO Device, Fixation, Proximal Femoral, Implant

All 22
Devices cleared under the same product code (JDO) and FDA review panel - the closest regulatory comparables to K964259.
INTERTAN CHS LOCKING PLATE SYSTEM PROX FEM PLATES/SCREW
K080434 · Smith & Nephew, Inc. · Apr 2008
GOTFRIED PERCUTANEOUS COMPRESSION PLATING SYSTEM
K983814 · Efratgo, Ltd. HI Tech Bio-Surgical · Jan 1999
SYNTHES (USA) DHS HELIX SYSTEM
K981757 · Synthes (Usa) · Jul 1998
VIGOR COMPRESSION HIP SCREW SYSTEM
K962644 · Deutschland Surgical, Inc. · Sep 1996
TITANIUM LIMITED CONTACT DYNAMIC HIP SCREW PLATE (TILC-DHS)
K953607 · Synthes (Usa) · Mar 1996
SYNTHES (USA) [SYNTHES] POINT CONTACT FIXATOR PLATE [PC-FIX]
K951904 · Synthes (Usa) · Jul 1995