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

LSF CEMENTED FEMORAL HIP

K Number: K902727 · Decision Aug 9, 1990
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
13
Review Days
49

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Basic Information

Device Name
LSF CEMENTED FEMORAL HIP
K Number
K902727
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Implant Technology, Inc.
Date Received
June 21, 1990
Decision Date
August 9, 1990
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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

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Other Clearances by Implant Technology, Inc.

K Number Device Name
K921525 HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESIS
K915617 LSF HA COATED FEMORAL HIP
K920021 LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUP
K913616 LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP
K901460 LSF(TM) TOTAL HIP SYSTEM
K891472 IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR
K884432 MODIFIED LSF TOTAL HIP SYSTEM
K883212 LSF (R) TOTAL HIP SYSTEM - BIPOLAR COMPONENT
K855017 LSF* TOTAL HIP SYSTEM
K841546 COMMUNI-TRACH TUBE
Search all 13 clearances from Implant Technology, Inc. →