Joint Medical Products Corp. - FDA 510(k) Cleared Devices
Recent clearances: ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP, S-ROM FEMORAL HIP STEM - SIZE 14 X 8, S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II
33
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Joint Medical Products Corp. Orthopedic ✕
33 devices
Cleared
Feb 26, 1996
ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP
Orthopedic
84d
Cleared
Jan 22, 1996
S-ROM FEMORAL HIP STEM - SIZE 14 X 8
Orthopedic
87d
Cleared
Aug 14, 1995
S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II
Orthopedic
346d
Cleared
Jun 21, 1995
S-ROM ZTP UHMWPE ACETABULAR CUP
Orthopedic
68d
Cleared
May 31, 1995
S-ROM OPC (ONE-PIECE CEMENTED) II FEMORAL HIP PROSTHESIS
Orthopedic
83d
Cleared
Apr 14, 1995
ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM
Orthopedic
42d
Cleared
Feb 01, 1995
KNEE PROTHESIS
Orthopedic
296d
Cleared
Oct 03, 1994
S-ROM NOILES CRUCIATE RETAINING KNEE
Orthopedic
287d
Cleared
Jun 03, 1994
COATED ZT PROXIMAL SLEEVE
Orthopedic
266d
Cleared
May 18, 1994
S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG
Orthopedic
407d
Cleared
Mar 09, 1994
S-ROM TOTAL HIP REPLACEMENT SYSTEM
Orthopedic
135d
Cleared
Mar 09, 1993
FEMORAL & TIBIAL AUGMENT BLOCK
Orthopedic
160d