Cleared Traditional

K934390 - OSCILLATING BONE SAW BLADE, 6200 SERIES

K934390 is an FDA 510(k) clearance for OSCILLATING BONE SAW BLADE, manufactured by Boehringer Laboratories. The device is a Class 1 General & Plastic Surgery device with product code GFA cleared through the Traditional 510(k) pathway after a 139-day FDA review.

K934390 · Boehringer Laboratories · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1994
Decision
139d
Days
Class 1
Risk

K934390 is an FDA 510(k) clearance for the OSCILLATING BONE SAW BLADE, 6200 SERIES. Classified as Blade, Saw, General & Plastic Surgery, Surgical (product code GFA), Class I - General Controls.

Submitted by Boehringer Laboratories (Norristown, US). The FDA issued a Cleared decision on January 26, 1994 after a review of 139 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4820 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Boehringer Laboratories devices

FDA 510(k) Submission Details - K934390

510(k) Number K934390 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 09, 1993
Decision Date January 26, 1994
Days to Decision 139 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
24d slower than avg
Panel avg: 115d · This submission: 139d
Pathway characteristics
Predicate-based equivalence.

GFA Device Classification - Class 1, General Controls

Product Code GFA Blade, Saw, General & Plastic Surgery, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4820
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GFA Blade, Saw, General & Plastic Surgery, Surgical

All 16
Devices cleared under the same product code (GFA) and FDA review panel - the closest regulatory comparables to K934390.
DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLS
K953012 · Boston Surgical Products, Inc. · Jul 1995
SURGICAL SAW BLADES
K950403 · Transidyne General Corp. · Feb 1995
SARNS STERNAL SAW II, STERNAL SAW II BLADE, SARNS SAW BLADES-NON-STERILE BULK PACK
K935391 · 3M Health Care, Sarns · Feb 1994
INTERMEDICS ORTHOPEDICS SAW BLADE
K931210 · Intermedics Orthopedics · Nov 1993
FLUID COOLED BONE SAW BLADE, 6000 SERIES
K924953 · Boehringer Laboratories · Jan 1993
MICRO-AIRE OSCILLATING SAW BLADE 202C-25, 202C-50
K896280 · Micro-Aire Surgical Instruments, Inc. · Nov 1989