Last synced on 14 November 2025 at 11:06 pm

Tera Lumbar Interbody Fusion System (Various PNs)

Page Type
Cleared 510(K)
510(k) Number
K251335
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2025
Days to Decision
33 days
Submission Type
Summary

Tera Lumbar Interbody Fusion System (Various PNs)

Page Type
Cleared 510(K)
510(k) Number
K251335
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2025
Days to Decision
33 days
Submission Type
Summary