Food and Drug Administration–reported complications of anatomic stemless total shoulder arthroplasty vary with implant model

Author:

Shah Nihar S.,Figueras Jorge H.ORCID,Hoge Connor G.ORCID,Sabbagh Ramsey S.ORCID,Grawe Brian M.

Publisher

Elsevier BV

Subject

Orthopedics and Sports Medicine,Surgery

Reference34 articles.

1. Risk factors for complications and revision surgery after anatomic and reverse total shoulder arthroplasty;Aibinder;J Shoulder Elbow Surg,2021

2. Association USFaD. 510(K) premarket notification. In: Association USFaD, ed. 11. US Food and Drug Administration: Silver Spring, MD.

3. Association USFaD. Classify your medical device: Download product code classifications files. In: Association USFaD, ed. US Food and Drug Administration: Silver Spring, MD.

4. Association USFaD. Manufacturer and user facility device experience database - (MAUDE) | FDA. In: Association USFaD, ed. US Food and Drug Administration: Silver Spring, MD.

5. Periprosthetic humeral fractures during shoulder arthroplasty;Athwal;J Bone Joint Surg Am,2009

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