Osteo Bos System in Stainless Steel

FDA 510(k) K973204 · Osteonics Corp.

Substantially Equivalent

510(k) numberK973204

Submission

Device name
Osteo Bos System in Stainless Steel
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
August 26, 1997
Decision date
September 25, 1997
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 Osteo Bos System in Stainless Steel cleared by the FDA?

Osteo Bos System in Stainless Steel (K973204) received a 510(k) decision of Substantially Equivalent on September 25, 1997, 30 days after the submission was received.

What is the product code of K973204?

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