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
1509721174
Device Listing 1509721174
Listing Summary
#
Listing key
1509721174
Premarket submission
K133091
Device
ZIP MIS INTERSPINOUS FUSION SYSTEM
Applicant
Aurora Spine
Product code
PEK
Decision date
2013-11-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
164775
3010326971
3010326971
AURORA SPINE, INC.
1
Y
2026-01-01
1930 Palomar Point Way Suite #103 Carlsbad CA US 92008
334838
3020417298
3020417298
Aurora Spine Manufacturing
1
N
2026-01-01
3146 Tiger Run Ct, Suite 116 Carlsbad CA US 92010