Idrives, Idrivec, Idrivef
FDA 510(k) K073001 · Power Medical Interventions, Inc.
510(k) numberK073001
Submission
- Device name
- Idrives, Idrivec, Idrivef
- Applicant
- Power Medical Interventions, Inc.
Langhorne, PA, US - Received
- October 24, 2007
- Decision date
- December 18, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GDW – Staple, Implantable
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4750
- Specialty
- General, Plastic Surgery
- Implant
- Yes
Other 510(k)s with product code GDW
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260196 | ETHICON Circular Stapler (CDH21mm); ETHICON Circular Stapler (CDH25mm); ETHICON…GDW · Traditional | Ethicon Endo-Surgery, LLC | 05/11/2026SE |
| K253657 | Tri-staple 2.0 Reloads; Endo GIA Reloads with Tri-Staple Technology; Endo GIA Gray…GDW · Traditional | Covidien (Part of Medtronic) | 04/10/2026SE |
| K252739 | ETHICON 4000 45mm Compact Stapler (EC3DT45C); ETHICON 4000 45mm Standard Stapler…GDW · Traditional | Ethicon Endo-Surgery, LLC | 12/17/2025SE |
| K250835 | ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm Standard Stapler…GDW · Traditional | Ethicon Endo-Surgery, LLC | 05/14/2025SE |
| K243276 | ECHELON LINEAR Stapler 30mm Stapler (GTX30); ECHELON LINEAR Stapler 60mm Stapler…GDW · Traditional | Ethicon Endo-Surgery, LLC | 02/25/2025SE |
| K241630 | ECHELON 4000 60mm Compact Stapler (EC3D60C); ECHELON 4000 60mm Standard Stapler…GDW · Traditional | Ethicon Endo-Surgery, LLC | 10/28/2024SE |
| K242679 | Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads (30mm…GDW · Special | Fengh Medical Co., Ltd. | 10/04/2024SE |
| K222487 | Anika Tissue Tack Fixation SystemGDW · Traditional | Anika Therapeutics, Inc. | 05/08/2023SE |
| K222210 | AEON Endoscopic StaplerGDW · Traditional | Lexington Medical, Inc. | 04/21/2023SE |
| K223760 | ECHELON LINEAR 60 mm Cutter (GLC60);ECHELON LINEAR 80mm Cutter (GLC80);ECHELON LINEAR…GDW · Traditional | Ethicon Endo-Surgery | 03/15/2023SE |
More from Ethicon Endo-Surgery
| 510(k) | Device | Decision |
|---|---|---|
| K091215 | Intelligent Power Unit, Intelligent Console, Intelligent Delivery System, Intelligent…GDW · Special | 05/18/2009SE |
| K083527 | Intelligent Articulating Endoscopic Linear Cutter Reverse with ReloadsGDW · Special | 12/18/2008SE |
| K081826 | Intelligent Straight and Articular Endoscopic Linear Cutters, Vascular with Reloads…GDW · Special | 07/25/2008SE |
| K073148 | Idrives, Idrivec, Idrivef with Vascular IndicationsGDW · Special | 12/07/2007SE |
| K071708 | I45, I45S, I60, and I60SGDW · Traditional | 09/27/2007SE |
| K063746 | Power Extenders Model# PEC200, PES200,PES200SGDW · Special | 01/12/2007SE |
| K063075 | Natural Orifice Linear Cutter Digital Loading UnitsGDW · Special | 11/02/2006SE |
| K061649 | Power Circular Stapler Digital Loading Unit with and Without SheathGDW · Special | 09/01/2006SE |
| K052910 | Power Right Angle Linear Cutter Digital Loading Unit with ReloadsGDW · Special | 11/07/2005SE |
| K052415 | Power Linear Cutter Reusable Digital Loading Units with ReloadsGDW · Special | 09/29/2005SE |
Questions and answers
When was Idrives, Idrivec, Idrivef cleared by the FDA?
Idrives, Idrivec, Idrivef (K073001) received a 510(k) decision of Substantially Equivalent on December 18, 2007, 55 days after the submission was received.
What is the product code of K073001?
The FDA product code is GDW – Staple, Implantable, a Class II (moderate risk) device regulated under 21 CFR 878.4750.