510(k) K823723

SPECTRON PROXIMAL FEMORAL PROSTHESIS by Richard'S Medical Equip., Inc. — Product Code JDI

K823723 is an FDA 510(k) premarket notification submitted by Richard'S Medical Equip., Inc. for the device "SPECTRON PROXIMAL FEMORAL PROSTHESIS". The FDA issued a decision of Substantially Equivalent on March 9, 1983. The device falls under product code JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented), a Class II device regulated under 21 CFR 888.3350. Richard'S Medical Equip., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 9, 1983
Date Received
December 10, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device Class
Class II
Regulation Number
888.3350
Review Panel
OR
Submission Type