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neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222988
510(k) Type
Traditional
Applicant
HT Medical d.b.a. Xenix Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2023
Days to Decision
338 days
Submission Type
Summary

neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222988
510(k) Type
Traditional
Applicant
HT Medical d.b.a. Xenix Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2023
Days to Decision
338 days
Submission Type
Summary