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
1395048615
Device Listing 1395048615
Listing Summary
#
Listing key
1395048615
Premarket submission
K170395
Device
TalosĀ® Lumbar (HA) PEEK IBF Devices
Applicant
Meditech Spine, LLC
Product code
MAX
Decision date
2017-06-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
144066
3009405289
3009405289
Meditech Spine, LLC
1
Y
2020-04-25
1447 Peachtree St NE Ste 440 Atlanta GA US 30309