FDA 510(k) Applications Submitted by TIMOTHY WILLIAMS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001044 | 03/31/2000 | ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM | ACME SPINE, LLC. |
| K010649 | 03/05/2001 | EXHALE DOPPLER SYSTEM | BRONCUS TECHNOLOGIES, INC. |
| K013111 | 09/18/2001 | EXHALE PROBE | BRONCUS TECHNOLOGIES, INC. |
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