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
1312328812
Device Listing 1312328812
Listing Summary
#
Listing key
1312328812
Premarket submission
K150468
Device
Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs
Applicant
K2 Medical GmbH & Co. KG
Product code
HAE
Decision date
2016-02-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13354
1056350
1000140363
BOSS INSTRUMENTS, LTD.
1
Y
2026-01-01
104 Sommerfield Drive Gordonsville VA US 22942