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

MEDICREA INTERNATIONAL ANTERIOR LUMBAR PLATE

K Number: K121323 · Decision Jul 18, 2012
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
17
Review Days
77

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MEDICREA INTERNATIONAL ANTERIOR LUMBAR PLATE
K Number
K121323
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea International
Date Received
May 2, 2012
Decision Date
July 18, 2012
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

View all

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 →