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
1363826607
Device Listing 1363826607
Listing Summary
#
Listing key
1363826607
Premarket submission
K203595
Device
DynaFuse Fixation System
Applicant
MedShape, Inc.
Product code
HWC
Decision date
2022-01-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
102152
3007593722
3007593722
MEDSHAPE, INC.
1
N
2026-01-01
1575 NORTHSIDE DR NW STE 440 Atlanta GA US 30318