The following data is part of a premarket notification filed by Disco-o-tech Medical Technologies, Ltd. with the FDA for Modification To Fixion Interlocking Proximal Femoral Intramedullary Nailing System.
Device ID | K012967 |
510k Number | K012967 |
Device Name: | MODIFICATION TO FIXION INTERLOCKING PROXIMAL FEMORAL INTRAMEDULLARY NAILING SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | DISCO-O-TECH MEDICAL TECHNOLOGIES, LTD. 3 HASADNOAT ST. Herzlia, IL 46728 |
Contact | Elad Magal |
Correspondent | Elad Magal DISCO-O-TECH MEDICAL TECHNOLOGIES, LTD. 3 HASADNOAT ST. Herzlia, IL 46728 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-09-04 |
Decision Date | 2001-10-04 |
Summary: | summary |