The following data is part of a premarket notification filed by Blackstone Medical, Inc. with the FDA for Blackstone Surgical Titanium Mesh System Angled End Rings.
Device ID | K032700 |
510k Number | K032700 |
Device Name: | BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | BLACKSTONE MEDICAL, INC. 90 BROOKSDALE DR. Springfield, MA 01104 |
Contact | Dean E Ciporkin |
Correspondent | Dean E Ciporkin BLACKSTONE MEDICAL, INC. 90 BROOKSDALE DR. Springfield, MA 01104 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-09-02 |
Decision Date | 2003-10-09 |
Summary: | summary |