Insignia Hip Stem, Restoration Modular 115mm Conical Distal Stem

FDA 510(k) K220731 · Stryker

Substantially Equivalent

510(k) numberK220731

Submission

Device name
Insignia Hip Stem, Restoration Modular 115mm Conical Distal Stem
Applicant
Stryker
Mahwah, NJ, US
Received
March 14, 2022
Decision date
August 11, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3353
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Insignia Hip Stem, Restoration Modular 115mm Conical Distal Stem cleared by the FDA?

Insignia Hip Stem, Restoration Modular 115mm Conical Distal Stem (K220731) received a 510(k) decision of Substantially Equivalent on August 11, 2022, 150 days after the submission was received.

What is the product code of K220731?

The FDA product code is MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, a Class II (moderate risk) device regulated under 21 CFR 888.3353.