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 |