The following data is part of a premarket notification filed by Ortho Solutions Limited with the FDA for Ortho Solutions - Sterile, Drills, Taps, Guide Pins & Wires.
Device ID | K102743 |
510k Number | K102743 |
Device Name: | ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRES |
Classification | Instrument, Surgical, Orthopedic, Ac-powered Motor And Accessory/attachment |
Applicant | ORTHO SOLUTIONS LIMITED 3150 EAST 200TH STREET Prior Lake, MN 55372 |
Contact | Al Lippincott |
Correspondent | Al Lippincott ORTHO SOLUTIONS LIMITED 3150 EAST 200TH STREET Prior Lake, MN 55372 |
Product Code | HWE |
Subsequent Product Code | GFA |
Subsequent Product Code | GFF |
Subsequent Product Code | HSZ |
CFR Regulation Number | 878.4820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-22 |
Decision Date | 2011-01-20 |
Summary: | summary |