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

WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014

K Number: K003618 · Decision May 23, 2001
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
13
Review Days
182

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Basic Information

Device Name
WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014
K Number
K003618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Whiteside Biomechanics, Inc.
Date Received
November 22, 2000
Decision Date
May 23, 2001
Product Code
NDD
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
NDD Cerclage, Fixation, Metallic

Other Clearances by Whiteside Biomechanics, Inc.

K Number Device Name
K033313 QUATRO M FEMORAL COMPONENT
K012800 SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
K993903 WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
K991678 WHITESIDE BIOMECHANICS SPINAL SYSTEM
K981238 BIPOLAR FEMORAL HEAD
K973261 WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD
K964616 QUATROLOC PLASMA SPRAYED FEMORAL COMPONENT
K971721 WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEAD
K971718 MICRO-SEAL ACETABULAR SYSTEM
K964150 WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEAD
Search all 13 clearances from Whiteside Biomechanics, Inc. →