FDA 510(k) Applications Submitted by OTIS BIOTECH CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K083077 | 10/16/2008 | ULC SPINAL PEDICLE SCREW SYSTEM | OTIS BIOTECH CO., LTD |
| K101472 | 05/27/2010 | MULTIFIT TOTAL HIP SYSTEM | OTIS BIOTECH CO., LTD |
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