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
1820033856
Device Listing 1820033856
Listing Summary
#
Listing key
1820033856
Premarket submission
K990657
Device
TRIFIX PEDICLE SPINAL SCREW ASSEMBLY
Applicant
Corin USA
Product code
MNH
Decision date
1999-03-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15439
9614209
3002806725
Lucinda Gerber
1
N
2026-01-01
480 Paramount Dr Raynham MA US 02767