Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by US SPINE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082801
09/24/2008
PHANTOM PLUS CAGE SYSTEM
US SPINE
K061041
04/14/2006
US SPINE FACET FIXATION SYSTEM
US SPINE
K081883
07/02/2008
MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM
US SPINE
K062785
09/18/2006
LTD POLYAXIAL FIXATION SYSTEM
US SPINE
K081296
05/07/2008
PREFERENCE PEDICLE SCREW SYSTEM
US SPINE
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact