The following data is part of a premarket notification filed by K2m with the FDA for K2m Navigation Instruments.
| Device ID | K171321 |
| 510k Number | K171321 |
| Device Name: | K2M Navigation Instruments |
| Classification | Orthopedic Stereotaxic Instrument |
| Applicant | K2M 600 Hope Parkway SE Leesburg, VA 20175 |
| Contact | Nancy Giezen |
| Correspondent | Nancy Giezen K2M 600 Hope Parkway SE Leesburg, VA 20175 |
| Product Code | OLO |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-05-04 |
| Decision Date | 2017-08-30 |
| Summary: | summary |