The following data is part of a premarket notification filed by Theken Spine Llc with the FDA for Stainless Steel Spinal System.
Device ID | K100970 |
510k Number | K100970 |
Device Name: | STAINLESS STEEL SPINAL SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | THEKEN SPINE LLC 1800 TRIPLETT BLVD. Akron, OH 44306 |
Contact | Dale Davison |
Correspondent | Dale Davison THEKEN SPINE LLC 1800 TRIPLETT BLVD. Akron, OH 44306 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-04-08 |
Decision Date | 2010-08-12 |
Summary: | summary |