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
1256818605
Device Listing 1256818605
Listing Summary
#
Listing key
1256818605
Premarket submission
K162604
Device
Cranial Reducing Tubes
Applicant
Medtronic Navigation, Inc.
Product code
HAW
Decision date
2016-12-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5808
1723170
1000517638
MEDTRONIC NAVIGATION, INC.
1
N
2026-01-01
200 Medtronic Drive Lafayette CO US 80026
312405
3018094310
3018094310
Medtronic Engineering and Innovation Center (MEIC)
1
N
2026-01-01
BSR Tech Park Survey No.135, 138, 141 & 142 Nanakramguda Main Hyderabad Telangana IN 500032