The following data is part of a premarket notification filed by Axon Instruments, Inc. with the FDA for Axon Mp-1 Micropositioner.
| Device ID | K990683 |
| 510k Number | K990683 |
| Device Name: | AXON MP-1 MICROPOSITIONER |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | AXON INSTRUMENTS, INC. 1101 CHESS DR. Foster City, CA 94404 -1102 |
| Contact | Andrew L Blatz |
| Correspondent | Andrew L Blatz AXON INSTRUMENTS, INC. 1101 CHESS DR. Foster City, CA 94404 -1102 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-03 |
| Decision Date | 1999-11-03 |
| Summary: | summary |