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
1617133344
Device Listing 1617133344
Listing Summary
#
Listing key
1617133344
Premarket submission
K233703
Device
Bone Anchor (NGS-BA-01)
Applicant
ClearPoint Neuro, Inc.
Product code
HAW
Decision date
2024-04-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
320627
3028006458
3028006458
ClearPoint Neuro Inc.
1
N
2026-01-01
6349 Paseo Del Lago Carlsbad CA US 92011