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

MODIFICATION TO TENOR SPINAL SYSTEM-ROD/BOLT CONNECTOR

K Number: K991528 · Decision May 28, 1999
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
56
Review Days
25

Basic Information

Device Name
MODIFICATION TO TENOR SPINAL SYSTEM-ROD/BOLT CONNECTOR
K Number
K991528
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DANEK MEDICAL, INC.
Date Received
May 3, 1999
Decision Date
May 28, 1999
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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