510(k) K953720

Device
Aesculap Caspar Plate & Screw System For Anterior Cervical Fusion
Applicant
AESCULAP, INC.
510(k) number
K953720
Product code
KWQ
Decision
Substantially Equivalent for Some Indications (SN)
Decision date
1995-11-02
Date received
1995-08-09
Regulation
888.3060
Classification name
Appliance, Fixation, Spinal Intervertebral Body
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
VICTORIA MACKINNON
Address
1000 Gateway Blvd. South San Francisco CA US 94080 94080

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KWQ#

510(k), Device, Applicant table
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