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
1543120290
Device Listing 1543120290
Listing Summary
#
Listing key
1543120290
Premarket submission
K062083
Device
SYNFIX -LR
Applicant
Synthes Spine Co.Lp
Product code
MQP
Decision date
2007-04-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
163675
3009996808
3009996808
SYNTHES USA PRODUCTS, LLC
1
N
2020-04-25
325 Paramount Drive Raynham MA US 02767