Cleared Traditional

K974537 - SYNTHES CANNULATED ANGLE BLADE PLATE (CABP) SYSTEM

K974537 is an FDA 510(k) clearance for SYNTHES CANNULATED ANGLE BLADE PLATE (C..., manufactured by Synthes (Usa). The device is a Class 2 Orthopedic device with product code KTT cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K974537 · Synthes (Usa) · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1998
Decision
77d
Days
Class 2
Risk

K974537 is an FDA 510(k) clearance for the SYNTHES CANNULATED ANGLE BLADE PLATE (CABP) SYSTEM. Classified as Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (product code KTT), Class II - Special Controls.

Submitted by Synthes (Usa) (Paoli, US). The FDA issued a Cleared decision on February 18, 1998 after a review of 77 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 - K974537

510(k) Number K974537 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1997
Decision Date February 18, 1998
Days to Decision 77 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
45d faster than avg
Panel avg: 122d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KTT Device Classification - Class 2, Special Controls

Product Code KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
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 - KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

All 358
Devices cleared under the same product code (KTT) and FDA review panel - the closest regulatory comparables to K974537.
EBI DFS JOINT FIXATOR, MODEL 02800
K981483 · Electro-Biology, Inc. · Jul 1998
BIOSYMMETRIC PROXIMAL INTERPHALANGEAL JOINT FIXATOR
K980370 · Biomet, Inc. · Apr 1998
FRIEDL GLIDING NAIL SYSTEM
K974409 · Plus Orthopedics · Feb 1998
THE CORIFIX DYNAMIC HIP SCREW SYSTEM
K973231 · Corin USA · Nov 1997
HOFFMANN II COMPACT PERIARTICULAR CLAMP
K973321 · Howmedica, Inc. · Nov 1997
ODI COMPRESSION HIP SCREW SYSTEM
K971993 · Orthopaedic Designs, Inc. · Nov 1997