The following data is part of a premarket notification filed by Brainlab Ag with the FDA for Brainlab Knee.
Device ID | K102990 |
510k Number | K102990 |
Device Name: | BRAINLAB KNEE |
Classification | Orthopedic Stereotaxic Instrument |
Applicant | BRAINLAB AG KAPELLENSTRASSE 12 Feldkirchen, DE 85622 |
Contact | Alexander Schwiersch |
Correspondent | Alexander Schwiersch BRAINLAB AG KAPELLENSTRASSE 12 Feldkirchen, DE 85622 |
Product Code | OLO |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-10-08 |
Decision Date | 2011-04-04 |
Summary: | summary |