510(k) K191963

SMR Finned Short Stems by Lima Corporate S.P.A. — Product Code MBF

K191963 is an FDA 510(k) premarket notification submitted by Lima Corporate S.P.A. for the device "SMR Finned Short Stems". The FDA issued a decision of Substantially Equivalent on October 10, 2019. The device falls under product code MBF (Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented), a Class II device regulated under 21 CFR 888.3670. Lima Corporate S.P.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 10, 2019
Date Received
July 23, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
Device Class
Class II
Regulation Number
888.3670
Review Panel
OR
Submission Type