The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Modification To Pyramid Anterior Plate Fixation System.
Device ID | K050117 |
510k Number | K050117 |
Device Name: | MODIFICATION TO PYRAMID ANTERIOR PLATE FIXATION SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Richard Treharne |
Correspondent | Richard Treharne MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-01-18 |
Decision Date | 2005-02-17 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00721902214240 | K050117 | 000 |
00721902214233 | K050117 | 000 |
00721902214219 | K050117 | 000 |
00721902214202 | K050117 | 000 |
00721902214196 | K050117 | 000 |