FDA FDA 510(k) clearance: corra® cervical plating system — K262149, Sep 24, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra cervical plating sys source ↗
FDA FDA 510(k) clearance: corra cervical plating system — K260570, Apr 22, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® cervical interbody system — K252894, Jan 6, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® cervical plating system — K252611, Dec 22, 2025. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion device; aprevo® anterior lumbar interbody fusion device with interfixation; aprevo® trans source ↗
FDA FDA 510(k) clearance: aprevo® posterior/transforaminal lumbar interbody fusion device — K250987, Jun 30, 2025. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation — K243802, Mar 17, 2025. Applicant at approval: Carl source ↗
FDA FDA 510(k) clearance: aprevo® Digital Planning — K242599, Dec 20, 2024. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® anterior lumbar interbody fusion device with interfixation — K243635, Dec 13, 2024. Applicant at approval: Carlsmed, Inc. source ↗
FDA FDA 510(k) clearance: aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM — K242260, Nov 15, 2024. Applicant at approval: Carlsmed, Inc. source ↗
FDA records (last 2 years)
FDA 510(k) clearance: corra® cervical plating system — K262149, Sep 24, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra cervical plating system — K260385, May 9, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: corra cervical plating system — K260570, Apr 22, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® cervical interbody system — K252894, Jan 6, 2026. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® cervical plating system — K252611, Dec 22, 2025. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® posterior/transforaminal lumbar interbody fusion device — K250987, Jun 30, 2025. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation — K243802, Mar 17, 2025. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® Digital Planning — K242599, Dec 20, 2024. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® anterior lumbar interbody fusion device with interfixation — K243635, Dec 13, 2024. Applicant at approval: Carlsmed, Inc. source ↗
FDA 510(k) clearance: aprevo® Cervical ACDF; aprevo® Cervical ACDF-X; aprevo® Cervical ACDF-X NO CAM — K242260, Nov 15, 2024. Applicant at approval: Carlsmed, Inc. source ↗
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