Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1437719545
Device Listing 1437719545
Listing Summary
#
Listing key
1437719545
Premarket submission
K090507
Device
MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM
Applicant
Ldr Spine USA
Product code
MAX
Decision date
2009-06-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
40504
8020776
4224
Michael van der Woude
1
N
2020-04-25
2500 Bee Cave Road Bldg 1, Suite 300 Austin TX US 78746