NAIL, INTRAMEDULLARY, FLEXIBLE

Rod, Fixation, Intramedullary And Accessories

DEPUY, INC.

The following data is part of a premarket notification filed by Depuy, Inc. with the FDA for Nail, Intramedullary, Flexible.

Pre-market Notification Details

Device IDK772081
510k NumberK772081
Device Name:NAIL, INTRAMEDULLARY, FLEXIBLE
ClassificationRod, Fixation, Intramedullary And Accessories
Applicant DEPUY, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHSB  
CFR Regulation Number888.3020 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1977-11-03
Decision Date1977-11-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.