The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc with the FDA for Crossfuse Ii Coronal Taper, Crossfuse Ii Hyperlordotic.
| Device ID | K133455 |
| 510k Number | K133455 |
| Device Name: | CROSSFUSE II CORONAL TAPER, CROSSFUSE II HYPERLORDOTIC |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
| Contact | Emily Downs |
| Correspondent | Emily Downs PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
| Product Code | MAX |
| Subsequent Product Code | MQP |
| Subsequent Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-11-12 |
| Decision Date | 2014-03-27 |
| Summary: | summary |