Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by CAROL CHANG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090839
03/27/2009
MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS
SYNTEC SCIENTIFIC CORP.
K101971
07/13/2010
SYNTEC OS SPINAL FIXATION SYSTEM
SYNTEC SCIENTIFIC CORP.
K092889
09/21/2009
SYNTEC OSTEO-PLATE AND SCREW FIXATION
SYNTEC SCIENTIFIC CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact