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FDA 510(k)

WILSON SPINAL FRAME

K-Number: K761036 · 1976-12-16

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1976-12-16
Product CodeHSQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WILSON SPINAL FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761036. The device is classified under product code HSQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON SPINAL FRAME?

WILSON SPINAL FRAME is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K761036.

When did WILSON SPINAL FRAME receive FDA 510(k) clearance?

WILSON SPINAL FRAME received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761036.

Who is the listed applicant for WILSON SPINAL FRAME?

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

What is the FDA product code for WILSON SPINAL FRAME?

The FDA product code for WILSON SPINAL FRAME is HSQ.

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Other records listing Orthopedic Equipment Co., 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.

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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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