Universal Bone Plate III System (Ubp III)

FDA 510(k) K020611 · Spinal Concepts, Inc.

Substantially Equivalent

510(k) numberK020611

Submission

Device name
Universal Bone Plate III System (Ubp III)
Applicant
Spinal Concepts, Inc.
Austin, TX, US
Received
February 25, 2002
Decision date
March 27, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Universal Bone Plate III System (Ubp III) cleared by the FDA?

Universal Bone Plate III System (Ubp III) (K020611) received a 510(k) decision of Substantially Equivalent on March 27, 2002, 30 days after the submission was received.

What is the product code of K020611?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.