The following data is part of a premarket notification filed by Orthopediatrics, Corp. with the FDA for Pedinail Intramedullary Nailing System.
Device ID | K083726 |
510k Number | K083726 |
Device Name: | PEDINAIL INTRAMEDULLARY NAILING SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | ORTHOPEDIATRICS, CORP. 210 N. BUFFALO ST. Warsaw, IN 46580 |
Contact | Gary Barnett |
Correspondent | Gary Barnett ORTHOPEDIATRICS, CORP. 210 N. BUFFALO ST. Warsaw, IN 46580 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-12-15 |
Decision Date | 2009-03-11 |
Summary: | summary |