Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K202467
Device Classification Name
Staple, Implantable
More FDA Info for this Device
510(K) Number
K202467
Device Name
Staple, Implantable
Applicant
Fengh Medical Co., Ltd.
D3 No. 6 Dongsheng West Road,
Jiangyin National High-tech Zone
Jiangyin 214437 CN
Other 510(k) Applications for this Company
Contact
Jiao Liu
Other 510(k) Applications for this Contact
Regulation Number
878.4750
More FDA Info for this Regulation Number
Classification Product Code
GDW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/27/2020
Decision Date
12/14/2020
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact