FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

OPTIMA SPINAL SYSTEM

K Number: K051971 · Decision Aug 4, 2005
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
12
Review Days
14

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Basic Information

Device Name
OPTIMA SPINAL SYSTEM
K Number
K051971
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
U&I Corp.
Date Received
July 21, 2005
Decision Date
August 4, 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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Other Clearances by U&I Corp.

K Number Device Name
K140864 VELOXTM INTERBODY FUSION SYSTEM
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K120419 DYNA LOCKING ANKLE NAIL
K112240 DYNA LOCKING CANNULATED SCREW
K102367 OPTIGEN TOTAL KNEE SYSTEM
K093707 DYNA LOCKING TROCHANTERIC NAIL, MODEL NG0820
K092771 DYNA LOCKING IM NAIL
K091725 PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549)
K061002 MAXIMA ANTERIOR CERVICAL PLATE SYSTEM
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