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FDA 510(k)

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

K-Number: K162702 · 2016-12-30

ApplicantStl International, Inc.
Decision Date2016-12-30
Product CodeHST
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is the device name listed in this FDA 510(k) record. The listed applicant is Stl International, Inc.. It received FDA 510(k) clearance on 2016-12-30 under 510(k) number K162702. The device is classified under product code HST. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is a medical device that received FDA 510(k) clearance on 2016-12-30. The listed applicant is Stl International, Inc.. The 510(k) number is K162702.

When did Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table receive FDA 510(k) clearance?

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table received FDA 510(k) clearance on 2016-12-30, under 510(k) number K162702.

Who is the listed applicant for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

The FDA 510(k) record lists Stl International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table?

The FDA product code for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table is HST.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT04488224Nano-X Image Guidance: CBCT With Gravity-induced MotionWITHDRAWN

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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