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

ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01

K Number: K031471 · Decision Oct 10, 2003
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
19
Review Days
154

Basic Information

Device Name
ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01
K Number
K031471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORTHOTEC, L.L.C.
Date Received
May 9, 2003
Decision Date
October 10, 2003
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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K Number Device Name
K040514 EOVIA CALCIUM PHOSPHATE CERAMIC
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K030958 ORIA SPINAL SYSTEM, DOMINO AND TUBE CONNECTORS
K023884 MODIFICATION ORIA SPINAL SYSTEM
K023378 ORIA CLARIS
K031452 ORIA SPINAL CLIP SYSTEM, SACRAL CONNECTOR, MODELS CA03 AND AO03
K030500 ORIA ZENITH
K023377 ORIA CERVICAL PLATES
K030252 ORIA SPINAL CLIP SYSTEM EXTENDED OMNIAXIAL CONNECTORS (CO05 & CO07)
K030253 ORIA SPINAL CLIP SYSTEM, LENGTHENED LATERAL CONNECTOR, MODEL AL06
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