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 |