Keyfix bone drill 9G 900204

Trade name

Keyfix bone drill 9G

Generic name

Bone access channel kit

Model / reference

900204

Primary DI / UDI-DI

08058964727718

FDA product code

HTW

GMDN term

Bone access channel kit

Device class

Class I

Regulation number

888.4540

GUDID distribution status

In Commercial Distribution

Category: Bone access channel kit

Other devices filed under FDA product code HTW (Bit, Drill).

• APEX Knee System 730010 by OMNIlife science, Inc.
• 4805-95-25 00-4805-095-25 by Zimmer, Inc.
• MARKED DRILL BIT 8163-01-009 816301009 by Biomet Orthopedics, Inc.
• XtraFix® 00-5207-025-10 by Zimmer, Inc.
• MaxMoreSpine 1001-BD 003B 1/2 by Hoogland Spine Products, GmbH
• LIGAFIX Router bit LIG9010572 by S.B.M
• ACUMED 80-4148 by ACUMED LLC
• NA IU 7427-20 by aap Implantate AG
• RetroTech Drill bit LIG9000294 by S.B.M
• APEX Knee System KR-55170 by OMNIlife science, Inc.

• KeyFix Direct Access Needle Trocar and bevel tip, 13 gauge 900106

  Class I

  GUDID on market

• Easy Winch 13 G, 15 mm 900222

  Class II

  FDA 510(k) K172214 Active Cleared 23 Aug 2017 GUDID on market

• Easy Winch 13 G, 10 mm 900221

  Class II

  FDA 510(k) K172214 Active Cleared 23 Aug 2017 GUDID on market

• Winch Kyphoplasty Balloon Catheter 15G 10 mm 900025

  Class II

  FDA 510(k) K172214 Active Cleared 23 Aug 2017 GUDID on market

See all devices from G21 SRL →