The following data is part of a premarket notification filed by Sofamor Danek Usa,inc. with the FDA for Colorado Ii Spinal System.
Device ID | K991031 |
510k Number | K991031 |
Device Name: | COLORADO II SPINAL SYSTEM |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Richard W Treharne |
Correspondent | Richard W Treharne SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | MNH |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-03-29 |
Decision Date | 2000-05-10 |
Summary: | summary |