510(k) K962101

ZWEYMUELLER SL FEMORAL HIP STEM by Intermedics Orthopedics — Product Code LZO

K962101 is an FDA 510(k) premarket notification submitted by Intermedics Orthopedics for the device "ZWEYMUELLER SL FEMORAL HIP STEM". The FDA issued a decision of Substantially Equivalent on August 19, 1996. The device falls under product code LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented), a Class II device regulated under 21 CFR 888.3353. Intermedics Orthopedics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 19, 1996
Date Received
May 30, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device Class
Class II
Regulation Number
888.3353
Review Panel
OR
Submission Type