The following data is part of a premarket notification filed by Corin Usa with the FDA for Optimized Positioning System (ops) Review.
Device ID | K193042 |
510k Number | K193042 |
Device Name: | Optimized Positioning System (OPS) ReView |
Classification | System, Image Processing, Radiological |
Applicant | Corin USA 12750 Citrus Park Lane Suite 120 Tampa, FL 33625 |
Contact | Lucinda Gerber |
Correspondent | Martina Cecconi Corin (Australia) 17 Bridge Street Sydney, AU 2073 |
Product Code | LLZ |
Subsequent Product Code | LWJ |
Subsequent Product Code | LZO |
Subsequent Product Code | MEH |
Subsequent Product Code | PLW |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-10-31 |
Decision Date | 2020-06-26 |