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
1895902464
Device Listing 1895902464
Listing Summary
#
Listing key
1895902464
Premarket submission
K260546
Device
Q Pedicle Instruments
Applicant
K2m, Inc.
Product code
OLO
Decision date
2026-03-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
338994
3004774118
3008599177
K2M, INC.
1
N
2026-01-01
600 Hope Pkwy SE Leesburg VA US 20175