The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc with the FDA for Pioneer Maxfuse Vertebral Body Replacement Device.
Device ID | K131724 |
510k Number | K131724 |
Device Name: | PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Contact | Emily M Downs |
Correspondent | Emily M Downs PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-12 |
Decision Date | 2013-12-24 |
Summary: | summary |