The following data is part of a premarket notification filed by Ortho Development with the FDA for Escalade Acetabular Cup System.
Device ID | K103384 |
510k Number | K103384 |
Device Name: | ESCALADE ACETABULAR CUP SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | ORTHO DEVELOPMENT 12187 S. BUSINESS PARK DR. Draper, UT 84020 |
Contact | Tom Haueter |
Correspondent | Tom Haueter ORTHO DEVELOPMENT 12187 S. BUSINESS PARK DR. Draper, UT 84020 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-11-18 |
Decision Date | 2011-03-16 |
Summary: | summary |