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

BLACKSTONE SPINAL FIXATION SYSTEM LATERAL OFFSET (SYSTEM MODIFICATION)

K Number: K030581 · Decision Jun 26, 2003
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
45
Review Days
122

Basic Information

Device Name
BLACKSTONE SPINAL FIXATION SYSTEM LATERAL OFFSET (SYSTEM MODIFICATION)
K Number
K030581
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BLACKSTONE MEDICAL, INC.
Date Received
February 24, 2003
Decision Date
June 26, 2003
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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