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

WHITESIDE BIOMECHANICS SPINAL SYSTEM

K Number: K991678 · Decision Aug 12, 1999
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
13
Review Days
87

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Basic Information

Device Name
WHITESIDE BIOMECHANICS SPINAL SYSTEM
K Number
K991678
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Whiteside Biomechanics, Inc.
Date Received
May 17, 1999
Decision Date
August 12, 1999
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

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Other Clearances by Whiteside Biomechanics, Inc.

K Number Device Name
K033313 QUATRO M FEMORAL COMPONENT
K012800 SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
K003618 WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014
K993903 WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
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. →