The following data is part of a premarket notification filed by Blackstone Medical, Inc. with the FDA for Blackstone Pedicle Screw System.
Device ID | K081684 |
510k Number | K081684 |
Device Name: | BLACKSTONE PEDICLE SCREW SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | BLACKSTONE MEDICAL, INC. 1211 HAMBURG TURNPIKE SUITE 300 Wayne, NJ 07470 |
Contact | Whitney G Torning |
Correspondent | Whitney G Torning BLACKSTONE MEDICAL, INC. 1211 HAMBURG TURNPIKE SUITE 300 Wayne, NJ 07470 |
Product Code | NKB |
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 | 2008-06-17 |
Decision Date | 2008-09-15 |
Summary: | summary |