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

TECHMEDICA STANDARD BIPOLAR SYSTEM

K Number: K925420 · Decision Sep 28, 1993
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
98
Applicant Total
31
Review Days
336

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Basic Information

Device Name
TECHMEDICA STANDARD BIPOLAR SYSTEM
K Number
K925420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3390
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Techmedica, Inc.
Date Received
October 27, 1992
Decision Date
September 28, 1993
Product Code
KWY
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
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Similar 510(k) Clearances

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

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Other Clearances by Techmedica, Inc.

K Number Device Name
K933935 CKS POROUS COATED FEMORAL COMPONENT
K932017 TECHMEDICA CONTINUUM HIP WITH HA COATING
K931929 TECHMEDICA CONTINUUM HIP SYSTEM
K926387 TECHMEDICA STANDARD CEMENTED HIP SYSTEM
K923808 MULLER STRAIGHT STEM FEMORAL PROSTHESIS
K926579 TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE
K911058 TECHMEDICA CAD/CAM CUSTOM HIP
K925181 TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
K920080 CONTINUUM KNEE SYSTEM
K921458 TMP MICROPLATING SYSTEM
Search all 31 clearances from Techmedica, Inc. →