The following data is part of a premarket notification filed by Ortho Development Corp. with the FDA for Pagoda Pedicle Screw System.
Device ID | K131785 |
510k Number | K131785 |
Device Name: | PAGODA PEDICLE SCREW SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | ORTHO DEVELOPMENT CORP. 12187 SOUTH BUSINESS PARK DR. Draper, UT 84020 |
Contact | Tom Haueter |
Correspondent | Tom Haueter ORTHO DEVELOPMENT CORP. 12187 SOUTH BUSINESS PARK DR. Draper, UT 84020 |
Product Code | NKB |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-18 |
Decision Date | 2013-08-20 |
Summary: | summary |