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

STELLA CERVICAL PLATE

K Number: K052763 · Decision Nov 10, 2005
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
12
Review Days
41

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Basic Information

Device Name
STELLA CERVICAL PLATE
K Number
K052763
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scient'X
Date Received
September 30, 2005
Decision Date
November 10, 2005
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

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K051063 POLYAXIAL HEMISPHERICAL SPINAL SCREWS
K043001 MX POLYAXIAL PEDICLE SCREW
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K042317 CERVICAL PLATE
K040747 ALADYN RIGID SPINE PLATE
K040454 BIOFILL BONE VOID FILLER
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