PALACOS R BONE CEMENT

FDA Premarket Approval P810020 S003

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DevicePALACOS R BONE CEMENT
Generic NameBone Cement
ApplicantSMITH & NEPHEW RICHARDS, INC.
Date Received1991-11-05
Decision Date1992-02-14
PMAP810020
SupplementS003
Product CodeLOD 
Advisory CommitteeOrthopedic
Supplement TypeNormal 180 Day Track
Supplement ReasonLabeling Change - Indications/instructions/shelf Life/tradename
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

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