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FDA 510(k)

GRAVITY TRACTION TABLE

K-Number: K851007 · 1985-06-21

ApplicantWilliam F. Trinkaus
Decision Date1985-06-21
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRAVITY TRACTION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is William F. Trinkaus. It received FDA 510(k) clearance on 1985-06-21 under 510(k) number K851007. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRAVITY TRACTION TABLE?

GRAVITY TRACTION TABLE is a medical device that received FDA 510(k) clearance on 1985-06-21. The listed applicant is William F. Trinkaus. The 510(k) number is K851007.

When did GRAVITY TRACTION TABLE receive FDA 510(k) clearance?

GRAVITY TRACTION TABLE received FDA 510(k) clearance on 1985-06-21, under 510(k) number K851007.

Who is the listed applicant for GRAVITY TRACTION TABLE?

The FDA 510(k) record lists William F. Trinkaus as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAVITY TRACTION TABLE?

The FDA product code for GRAVITY TRACTION TABLE is INQ.

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Related Devices (Code: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

Official Source

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

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