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

Adena-Zina System

K Number: K212066 · Decision Aug 16, 2021
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
9
Review Days
45

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
Adena-Zina System
K Number
K212066
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai Sanyou Medical Co, Ltd.
Date Received
July 2, 2021
Decision Date
August 16, 2021
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

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

View all

Other Clearances by Shanghai Sanyou Medical Co, Ltd.

K Number Device Name
K230872 Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar Cage System, KEYSTONE Cage System
K230961 Zeus Spinal System
K231931 Adena-Zina Spinal System
K211689 KEYSTONE PEEK Cage System
K163366 Shanghai Sanyou CARMEN Cervical Fusion System
K163422 Shanghai Sanyou PEEK Cage System
K152781 Adena-Zina System
K131512 KATIA SYSTEM