SCS Claris Spinal Screws, Types V,G,E

FDA 510(k) K011807 · Ortho Tec, LLC

Substantially Equivalent

510(k) numberK011807

Submission

Device name
SCS Claris Spinal Screws, Types V,G,E
Applicant
Ortho Tec, LLC
Chesterland, OH, US
Received
June 11, 2001
Decision date
August 7, 2001
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNI – Orthosis, Spinal Pedicle Fixation
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3070
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was SCS Claris Spinal Screws, Types V,G,E cleared by the FDA?

SCS Claris Spinal Screws, Types V,G,E (K011807) received a 510(k) decision of Substantially Equivalent on August 7, 2001, 57 days after the submission was received.

What is the product code of K011807?

The FDA product code is MNI – Orthosis, Spinal Pedicle Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.