The following data is part of a premarket notification filed by Tornier Inc. with the FDA for Ortholoc Sps Shoulder Plating System.
Device ID | K181587 |
510k Number | K181587 |
Device Name: | ORTHOLOC SPS Shoulder Plating System |
Classification | Plate, Fixation, Bone |
Applicant | Tornier Inc. 10801 Nesbitt Ave South Bloomington, MN 55437 |
Contact | Renee Stoffel |
Correspondent | Renee Stoffel Tornier Inc. 10801 Nesbitt Ave South Bloomington, MN 55437 |
Product Code | HRS |
Subsequent Product Code | HWC |
Subsequent Product Code | KTT |
Subsequent Product Code | KTW |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-06-15 |
Decision Date | 2018-10-05 |
Summary: | summary |