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FDA 510(k)

TLC SUPPORT PRODUCTS

K-Number: K803029 · 1980-12-22

ApplicantOrthopedic Systems, Inc.
Decision Date1980-12-22
Product Code
DecisionSubstantially Equivalent

Device Summary

TLC SUPPORT PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K803029. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TLC SUPPORT PRODUCTS?

TLC SUPPORT PRODUCTS is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K803029.

When did TLC SUPPORT PRODUCTS receive FDA 510(k) clearance?

TLC SUPPORT PRODUCTS received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803029.

Who is the listed applicant for TLC SUPPORT PRODUCTS?

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

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.

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Other records listing Orthopedic Systems, Inc. as applicant

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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910736JACKSON MULTIPURPOSE OPERATING TABLEK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEE

View all 95 devices →

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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