Re-Sharpenable Saw Blades

FDA 510(k) K940501 · Adven Medical

Substantially Equivalent

510(k) numberK940501

Submission

Device name
Re-Sharpenable Saw Blades
Applicant
Adven Medical
Plymouth, MN, US
Received
February 2, 1994
Decision date
June 28, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GFA – Blade, Saw, General & Plastic Surgery, Surgical
Device class
Class I (low risk)
Regulation
21 CFR 878.4820
Specialty
General, Plastic Surgery

Other 510(k)s with product code GFA

510(k)DeviceApplicantDecision
K971978Graft Harvesting SawbladesGFA · Traditional Wrightmedicaltechnologyinc06/18/1997SE
K954483Stryker Sagittal Saw AttachmentGFA · Traditional Stryker Instruments01/30/1996SE
K955229Wright Medical Technology SawbladesGFA · Traditional Wrightmedicaltechnologyinc01/18/1996SE
K953012Disposable & Reusable Surgical Cutting ToolsGFA · Traditional Boston Surgical Products, Inc.07/12/1995SE
K950403Surgical Saw BladesGFA · Traditional Transidyne General Corp.02/21/1995SE
K933595Bur, Surgical, General & Plastic SurgeryGFA · Traditional Omega Surgical Instruments, Inc.03/16/1994SE
K935391Sarns Sternal Saw II, Sternal Saw II Blade, Sarns Saw Blades-Non-Sterile Bulk PackGFA · Traditional 3M Health Care, Sarns02/24/1994SE
K934603Surgical Saw BladesGFA · Traditional American Medical Specialties, Inc.02/22/1994SE
K931769Snap Oscillating SawGFA · Traditional Surgiquip, Inc.01/27/1994SE
K934390Oscillating Bone Saw Blade, 6200 SeriesGFA · Traditional Boehringer Laboratories01/26/1994SE

More from Boehringer Laboratories

510(k)DeviceDecision
K021528Reprocessed Venodyne Sequential Compression Sleeves / WrapJOW · Traditional 08/21/2002SE
K013987Reprocessed Disposable TrocarsKBG · Traditional 03/01/2002SE
K012675Reprocessed Used Disposable Sequential Compression Sleeves/WrapsJOW · Traditional 02/12/2002SE
K012694Reprocessed Used Disposable Arthroscopic Blades and BursHWE · Traditional 02/04/2002SE
K012676Reprocessed Used, Disposable Blades, Burs, Bits and TapsHWE · Traditional 02/04/2002SE

Questions and answers

When was Re-Sharpenable Saw Blades cleared by the FDA?

Re-Sharpenable Saw Blades (K940501) received a 510(k) decision of Substantially Equivalent on June 28, 1994, 146 days after the submission was received.

What is the product code of K940501?

The FDA product code is GFA – Blade, Saw, General & Plastic Surgery, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4820.