FDA 510(k) Applications for Medical Device Product Code "MRI"
(Orthosis, Truncal/Orthosis, Limb)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K923880 | MOPAC, LTD. | ORLAU SWIVEL WALKER | 09/30/1996 |
| K973031 | R. THOMAS GROTZ, M.D., INC. | STABILIZER SOFT TISSUE ANCHOR 5MM MODEL TA1005, ANCHOR INSERTER/SUTURE ORGANIZER 5MM AI1005, STABILIZER DRILL 5MM NONSTE | 11/03/1997 |
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