Dynasty Acetabular Shell; Dynasty A-Class Poly Acetabular Liner

FDA 510(k) K061547 · Wrightmedicaltechnologyinc

Substantially Equivalent

510(k) numberK061547

Submission

Device name
Dynasty Acetabular Shell; Dynasty A-Class Poly Acetabular Liner
Applicant
Wrightmedicaltechnologyinc
Arlington, TN, US
Received
June 5, 2006
Decision date
July 3, 2006
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3358
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Dynasty Acetabular Shell; Dynasty A-Class Poly Acetabular Liner cleared by the FDA?

Dynasty Acetabular Shell; Dynasty A-Class Poly Acetabular Liner (K061547) received a 510(k) decision of Substantially Equivalent on July 3, 2006, 28 days after the submission was received.

What is the product code of K061547?

The FDA product code is LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3358.