Lactosorb Trauma Plating System

FDA 510(k) K992355 · Biomet, Inc.

Substantially Equivalent

510(k) numberK992355

Submission

Device name
Lactosorb Trauma Plating System
Applicant
Biomet, Inc.
Warsaw, IN, US
Received
July 14, 1999
Decision date
December 20, 1999
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 Lactosorb Trauma Plating System cleared by the FDA?

Lactosorb Trauma Plating System (K992355) received a 510(k) decision of Substantially Equivalent on December 20, 1999, 159 days after the submission was received.

What is the product code of K992355?

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