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

KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM

K Number: K922824 · Decision Sep 17, 1992
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
113
Applicant Total
33
Review Days
98

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Basic Information

Device Name
KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM
K Number
K922824
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Joint Medical Products Corp.
Date Received
June 11, 1992
Decision Date
September 17, 1992
Product Code
HSX
Advisory Committee
Orthopedic
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

Similar 510(k) Clearances

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

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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. →