510(k) K210998

ROSA Hip System by Orthosoft D/B/A Zimmer Cas — Product Code LLZ

K210998 is an FDA 510(k) premarket notification submitted by Orthosoft D/B/A Zimmer Cas for the device "ROSA Hip System". The FDA issued a decision of Substantially Equivalent on August 17, 2021. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Orthosoft D/B/A Zimmer Cas has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 17, 2021
Date Received
April 2, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type