The following data is part of a premarket notification filed by Blackstone Medical, Inc. with the FDA for Blackstone Pillar Xl Peek Spacers.
| Device ID | K082235 |
| 510k Number | K082235 |
| Device Name: | BLACKSTONE PILLAR XL PEEK SPACERS |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| 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 | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-07 |
| Decision Date | 2008-09-04 |
| Summary: | summary |