FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

PASS OCT SPINAL SYSTEM

K Number: K121979 · Decision Mar 21, 2013
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
17
Review Days
258

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Basic Information

Device Name
PASS OCT SPINAL SYSTEM
K Number
K121979
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International
Date Received
July 6, 2012
Decision Date
March 21, 2013
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

Similar 510(k) Clearances

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Other Clearances by Medicrea International

K Number Device Name
K220810 Infinity™ OCT System and PASS OCT Spinal System
K220724 CD Horizon™ Spinal System and PASS LP™ Spinal System
K180091 UNiD Spine Analyzer
K170172 UNiD Spine Analyzer
K153169 PASS OCT Patient Specific Rods
K150049 PASS LP Spinal System
K140738 PASS LP SPINAL SYSTEM
K133906 C-JAWS CERVICAL COMPRESSIVE STAPLE
K132395 LIGAPASS
K132574 PASS LP SPINAL SYSTEM
Search all 17 clearances from Medicrea International →