WASTON Metallic Bone Plate and Screw Systems

FDA 510(k) K151057 · Changzhou Waston Medical Appliance Co., Ltd.

Substantially Equivalent

510(k) numberK151057

Submission

Device name
WASTON Metallic Bone Plate and Screw Systems
Applicant
Changzhou Waston Medical Appliance Co., Ltd.
Changzhou, CN
Received
April 20, 2015
Decision date
August 10, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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More from Bonebridge AG

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K151062WASTON Metallic Intramedullary Nail SystemHSB · Traditional 12/17/2015SE
K150684WASTON General Spinal SystemMNI · Traditional 11/18/2015SE
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Questions and answers

When was WASTON Metallic Bone Plate and Screw Systems cleared by the FDA?

WASTON Metallic Bone Plate and Screw Systems (K151057) received a 510(k) decision of Substantially Equivalent on August 10, 2015, 112 days after the submission was received.

What is the product code of K151057?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.