The following data is part of a premarket notification filed by Danek Medical, Inc. with the FDA for Modification Of Tsrh Spinal System.
Device ID | K984522 |
510k Number | K984522 |
Device Name: | MODIFICATION OF TSRH SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | DANEK MEDICAL, INC. 1800 PYRAMID PL. Memphis, TN 38132 |
Contact | Richard W Treharne |
Correspondent | Richard W Treharne DANEK MEDICAL, INC. 1800 PYRAMID PL. Memphis, TN 38132 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-12-21 |
Decision Date | 1999-01-06 |
Summary: | summary |