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

MODIFICATION TO PASSMED SPINAL SYSTEM

K Number: K070530 · Decision Oct 18, 2007
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
14
Review Days
237

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Basic Information

Device Name
MODIFICATION TO PASSMED SPINAL SYSTEM
K Number
K070530
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicrea Technologies
Date Received
February 23, 2007
Decision Date
October 18, 2007
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

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Other Clearances by Medicrea Technologies

K Number Device Name
K102406 PASS ANTERIOR SPINAL SYSTEM
K100544 IMPIX LUMBAR INTERBODY DEVICE
K083798 IMPIX ALIF LUMBAR IBF, IMPIX ALIF-D LUMBAR IBF, IMPIX TLIF LUMBAR IBF
K100297 PASS LP SPINAL SYSTEM
K083810 PASS LP SPINAL SYSTEM
K083308 PASS LP SPINAL SYSTEM
K082069 PASS 2 SPINAL SYSTEM
K082577 PASS LP SPINAL SYSTEM
K080099 PASS SPINAL SYSTEM
K072226 IMPIX SPACER
Search all 14 clearances from Medicrea Technologies →