510(k) K951356

VARIOUS UHMWP HIP & KNEE JOINT PROSTHESIS MODIFIED by Biologically Oriented Prostheses — Product Code LPH

K951356 is an FDA 510(k) premarket notification submitted by Biologically Oriented Prostheses for the device "VARIOUS UHMWP HIP & KNEE JOINT PROSTHESIS MODIFIED". The FDA issued a decision of SN on June 19, 1995. The device falls under product code LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented), a Class II device regulated under 21 CFR 888.3358. Biologically Oriented Prostheses has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
June 19, 1995
Date Received
March 24, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device Class
Class II
Regulation Number
888.3358
Review Panel
OR
Submission Type