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
2039007606
Device Listing 2039007606
Listing Summary
#
Listing key
2039007606
Premarket submission
K173411
Device
Comprehensive Segmental Revision System (SRS)
Applicant
Biomet Manufacturing Corp
Product code
PHX
Decision date
2018-02-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
215587
3014315560
3014315560
Zimmer Biomet Centroamerica SA
1
N
2026-01-01
Oficentro Ejecutivo La Sabana Edificio 7, Piso 3 san jose CR 10101