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

PASS OCT Patient Specific Rods

K Number: K153169 · Decision Jan 29, 2016
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
17
Review Days
88

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Basic Information

Device Name
PASS OCT Patient Specific Rods
K Number
K153169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International
Date Received
November 2, 2015
Decision Date
January 29, 2016
Product Code
NKG
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
NKG Posterior Cervical Screw System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKG), ordered by most recent decision date.

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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
K150049 PASS LP Spinal System
K140738 PASS LP SPINAL SYSTEM
K133906 C-JAWS CERVICAL COMPRESSIVE STAPLE
K132395 LIGAPASS
K132574 PASS LP SPINAL SYSTEM
K132575 PASS LP SPINAL SYSTEM
Search all 17 clearances from Medicrea International →