Lactosorb Panels and Fasteners

FDA 510(k) K984390 · Biomet, Inc.

Substantially Equivalent

510(k) numberK984390

Submission

Device name
Lactosorb Panels and Fasteners
Applicant
Biomet, Inc.
Warsaw, IN, US
Received
December 8, 1998
Decision date
August 7, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 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 Panels and Fasteners cleared by the FDA?

Lactosorb Panels and Fasteners (K984390) received a 510(k) decision of Substantially Equivalent on August 7, 2000, 608 days after the submission was received.

What is the product code of K984390?

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