FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

METALLIC LOCKING COMPRESSION BONE PLATES AND SCREWS SYSTEM

K Number: K131759 · Decision Aug 8, 2013
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
3
Review Days
52

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
METALLIC LOCKING COMPRESSION BONE PLATES AND SCREWS SYSTEM
K Number
K131759
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tianjin Walkman Biomaterial Co., Ltd.
Date Received
June 17, 2013
Decision Date
August 8, 2013
Product Code
HRS
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRS Plate, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HRS), ordered by most recent decision date.

View all

Other Clearances by Tianjin Walkman Biomaterial Co., Ltd.

K Number Device Name
K140229 GENERAL SPINAL SYSTEM
K132078 METALLIC INTRAMEDULLARY NAIL SYSTEM