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510(k) K915385

Device
PPC HIP STEM COMPONENT
Applicant
IMPLANTOLOGY CORP.
510(k) number
K915385
Product code
JDG  
Decision
Substantially Equivalent For Some Indications (SN)
Decision date
1993-05-17
Date received
1991-11-29
Regulation
888.3360
Classification name
Prosthesis, Hip, Femoral Component, Cemented, Metal
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
MARK FORTE
Address
11 Oak Ln. Pine Brook NJ US 07058 07058

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JDG  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.2022-02-07
K193546Distal CentralizersBiomet, Inc.2020-09-25
K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker Orthopaedics2018-03-19
K001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast Company2000-09-27
K992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USA1999-11-10
K962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, Inc.1996-08-08
K955171NEXLOCK FEMORAL STEMNexmed, Inc.1996-02-09
K953653LUBINUS SP II HIP SYSTEMTurnkey Intergration USA, Inc.1995-11-06
K953067HIP FRACTURE STEM FENESTRATION PLUGHowmedica Corp.1995-08-21
K945783ORTHOMET TITANIUM HYBRID FEMORAL STEMOrthomet, Inc.1995-05-30
K951083PROFORM CEMENTED FEMORAL COMPONENTStelkast Company1995-05-22
K942479INTEGRAL CO-CR FEMORAL COMPONENTBiomet, Inc.1994-09-20
K942028RX90 FEMORAL COMPONENTBiomet, Inc.1994-09-19
K942027IMPACT CO-CR 1-PIECE FEMORAL COMPONENTBiomet, Inc.1994-09-19
K931194CO-CR ANSWER FEMORAL COMPONENTBiomet, Inc.1994-05-05

Legacy Summary#

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FDA Review#

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