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
1086761684
Device Listing 1086761684
Listing Summary
#
Listing key
1086761684
Premarket submission
K960356
Device
POSTERIOR ANNULOPLASTY BAND (MODEL 607)
Applicant
The Heart Valve Div. Medtronic Cardiovascular Surg
Product code
KRH
Decision date
1996-08-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5821
2025587
2025587
Medtronic Heart Valves Division
1
N
2026-01-01
1851 EAST DEERE AVE. Santa Ana CA US 92705
5793
9617601
3002534070
Celia Encinas
1
N
2026-01-01
1610 Landmark Rd San Diego CA US 92154
230369
3015544746
3015544746
Medtronic, Inc.
1
N
2026-01-01
7000 Central Ave., N.E. Minneapolis MN US 55432