PALACOS R BONE CEMENT

FDA Premarket Approval P810020

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DevicePALACOS R BONE CEMENT
Generic NameBone Cement
ApplicantSMITH & NEPHEW RICHARDS, INC.
Date Received1981-05-13
Decision Date1984-02-02
Notice Date1984-02-28
PMAP810020
SupplementS
Product CodeLOD 
Docket Number84M-0053
Advisory CommitteeOrthopedic
Expedited ReviewNo
Combination Product No
Applicant Address SMITH & NEPHEW RICHARDS, INC. 1450 Brooks Rd. memphis, TN 38116

Supplemental Filings

Supplement NumberDateSupplement Type
P810020Original Filing
S005 1998-09-14 Real-time Process
S004 1995-07-20 Normal 180 Day Track
S003 1991-11-05 Normal 180 Day Track
S002 1988-12-12 Normal 180 Day Track
S001 1984-06-04

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.