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

MODIFICATION ORIA SPINAL SYSTEM

K Number: K023884 · Decision Aug 20, 2003
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
22
Review Days
272

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Basic Information

Device Name
MODIFICATION ORIA SPINAL SYSTEM
K Number
K023884
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Tec, LLC
Date Received
November 21, 2002
Decision Date
August 20, 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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Other Clearances by Ortho Tec, LLC

K Number Device Name
K040514 EOVIA CALCIUM PHOSPHATE CERAMIC
K040346 MODIFICATION TO ORIA TOP CLIP SYSTEM
K030958 ORIA SPINAL SYSTEM, DOMINO AND TUBE CONNECTORS
K031471 ORIA SPINAL CLIP SYSTEM, LATERAL INTERMEDIATE CONNECTOR, MODEL AL01
K023378 ORIA CLARIS
K031452 ORIA SPINAL CLIP SYSTEM, SACRAL CONNECTOR, MODELS CA03 AND AO03
K030500 ORIA ZENITH
K023377 ORIA CERVICAL PLATES
K030253 ORIA SPINAL CLIP SYSTEM, LENGTHENED LATERAL CONNECTOR, MODEL AL06
K030252 ORIA SPINAL CLIP SYSTEM EXTENDED OMNIAXIAL CONNECTORS (CO05 & CO07)
Search all 22 clearances from Ortho Tec, LLC →