FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

S-ROM(TM) FEMORAL STEM CENTRALIZER/CEMENT SPACER

K Number: K904746 · Decision Nov 20, 1990
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
53
Applicant Total
33
Review Days
33

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
S-ROM(TM) FEMORAL STEM CENTRALIZER/CEMENT SPACER
K Number
K904746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Joint Medical Products Corp.
Date Received
October 18, 1990
Decision Date
November 20, 1990
Product Code
JDK
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JDK Prosthesis, Hip, Cement Restrictor

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDK), ordered by most recent decision date.

View all

Other Clearances by Joint Medical Products Corp.

K Number Device Name
K955511 ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP
K954935 S-ROM FEMORAL HIP STEM - SIZE 14 X 8
K944321 S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II
K951726 S-ROM ZTP UHMWPE ACETABULAR CUP
K951084 S-ROM OPC (ONE-PIECE CEMENTED) II FEMORAL HIP PROSTHESIS
K951000 ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM
K941769 KNEE PROTHESIS
K936037 S-ROM NOILES CRUCIATE RETAINING KNEE
K934412 COATED ZT PROXIMAL SLEEVE
K931676 S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG
Search all 33 clearances from Joint Medical Products Corp. →