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Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162702
510(k) Type
Traditional
Applicant
STL International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2016
Days to Decision
93 days
Submission Type
Summary

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162702
510(k) Type
Traditional
Applicant
STL International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2016
Days to Decision
93 days
Submission Type
Summary