The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for Ortholoc 3di Ankle Plating System, Ortholoc Bone Screw.
Device ID | K102429 |
510k Number | K102429 |
Device Name: | ORTHOLOC 3DI ANKLE PLATING SYSTEM, ORTHOLOC BONE SCREW |
Classification | Plate, Fixation, Bone |
Applicant | WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Contact | Megan Mccagh |
Correspondent | Megan Mccagh WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. Arlington, TN 38002 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-25 |
Decision Date | 2010-11-23 |
Summary: | summary |