Depuy Synthes Inhanceв ў Shoulder System Receives Fda 510 K Clearance

Depuy Synthes Inhanceв ў Shoulder System Receives Fda 5 Warsaw, in – may 16, 2022 – today, johnson & johnson medtech* announced that the inhance™ shoulder system from depuy synthes, the orthopaedics company of johnson & johnson,** has received 510(k) clearance from the u.s. food and drug administration (fda) for use in reverse total shoulder arthroplasty procedures. this clearance is in. Depuy synthes has announced fda 510(k) clearance for the inhance shoulder system for use in reverse total shoulder arthroplasty procedures, according to a press release.the inhance system, which.

Inhanceв ў Shoulder System Depuy Synthes Depuy synthes inhance™ shoulder system receives fda 510(k) clearance for use in reverse total shoulder arthroplasty johnson & johnson medtech* has announced that the inhance™ shoulder system from depuy synthes, the orthopaedics company of johnson & johnson,** has received 510(k) clearance from the u.s. food and drug. The u.s. food and drug administration (fda) has granted 510 (k) clearance to the depuy synthes inhance™ shoulder system for use in shoulder replacement procedures. according to the fda 510 (k) document, the inhance shoulder system reverse total shoulder with a humeral stem is indicated for “primary, fracture or revision total reverse. May 31, 2022. depuy synthes’s inhance shoulder system has received an expanded 510 (k) clearance from the fda for use in reverse total shoulder arthroplasty procedures. the agency previously cleared the system for use anatomic shoulder arthroplasty. reverse total shoulder arthroplasty involves replacing the rounded head of the upper arm bone. Warsaw, in – may 16, 2022 – today, johnson & johnson medtech* announced that the inhance™ shoulder system from depuy synthes, the orthopaedics company of johnson & johnson,** has received 510(k) clearance from the u.s. food and drug administration (fda) for use in reverse total shoulder arthroplasty procedures. this clearance is in.