The following data is part of a premarket notification filed by Blackstone Medical, Inc. with the FDA for Construx Pl/tl Peek Partial Vbr System.
Device ID | K060350 |
510k Number | K060350 |
Device Name: | CONSTRUX PL/TL PEEK PARTIAL VBR SYSTEM |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | BLACKSTONE MEDICAL, INC. 1211 HAMBURG TURNPIKE SUITE 300 Wayne, NJ 07470 |
Contact | Whitney G Turning |
Correspondent | Whitney G Turning BLACKSTONE MEDICAL, INC. 1211 HAMBURG TURNPIKE SUITE 300 Wayne, NJ 07470 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-02-10 |
Decision Date | 2006-02-24 |
Summary: | summary |