Xcision Medical Systems, LLC
Xcision Medical Systems, LLC holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2018, with 2 FDA device recalls on record.
Top product codes for Xcision Medical Systems, LLC
FDA recalls by Xcision Medical Systems, LLC
- Z-0750-2024 — GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.
- Z-2081-2019 — GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Xcision Medical Systems, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.