The following data is part of a premarket notification filed by Theken Surgical with the FDA for Coral Spinal System.
Device ID | K041592 |
510k Number | K041592 |
Device Name: | CORAL SPINAL SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | THEKEN SURGICAL 283 E. WATERLOO ROAD Akron, OH 44203 |
Contact | Randy Theken |
Correspondent | Randy Theken THEKEN SURGICAL 283 E. WATERLOO ROAD Akron, OH 44203 |
Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
Subsequent Product Code | NKB |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-06-14 |
Decision Date | 2004-09-16 |
Summary: | summary |