The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc with the FDA for Pioneer Lateral Plate System.
Device ID | K120724 |
510k Number | K120724 |
Device Name: | PIONEER LATERAL PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Contact | Sarah Mcintyre |
Correspondent | Sarah Mcintyre PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-09 |
Decision Date | 2012-05-07 |
Summary: | summary |