The following data is part of a premarket notification filed by Pioneer Surgical Technology with the FDA for Quantum Spinal System, Quantum Mis.
Device ID | K101790 |
510k Number | K101790 |
Device Name: | QUANTUM SPINAL SYSTEM, QUANTUM MIS |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | PIONEER SURGICAL TECHNOLOGY 5 HEMINGWAY LANE West Newbury, MA 01985 |
Contact | Barry E Sands |
Correspondent | Barry E Sands PIONEER SURGICAL TECHNOLOGY 5 HEMINGWAY LANE West Newbury, MA 01985 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-28 |
Decision Date | 2011-03-07 |
Summary: | summary |