The following data is part of a premarket notification filed by Spinal Usa with the FDA for Modification To: Pss System.
Device ID | K092128 |
510k Number | K092128 |
Device Name: | MODIFICATION TO: PSS SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | SPINAL USA 2050 EXECUTIVE DR. Pearl, MS 39208 |
Contact | Jeffrey Johnson |
Correspondent | Jeffrey Johnson SPINAL USA 2050 EXECUTIVE DR. Pearl, MS 39208 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-07-15 |
Decision Date | 2009-09-14 |
Summary: | summary |