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

PASS LP SPINAL SYSTEM

K Number: K132574 · Decision Nov 8, 2013
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
18
Applicant Total
17
Review Days
84

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Basic Information

Device Name
PASS LP SPINAL SYSTEM
K Number
K132574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International
Date Received
August 16, 2013
Decision Date
November 8, 2013
Product Code
OSH
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
OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

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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
K132575 PASS LP SPINAL SYSTEM
Search all 17 clearances from Medicrea International →