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FDA 510(k)

THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC

K-Number: K802271 · 1980-10-23

ApplicantThe Anspach Effort, Inc.
Decision Date1980-10-23
Product CodeBWN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802271. The device is classified under product code BWN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC?

THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K802271.

When did THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC receive FDA 510(k) clearance?

THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802271.

Who is the listed applicant for THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC?

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

What is the FDA product code for THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC?

The FDA product code for THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC is BWN.

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Other records listing The Anspach Effort, 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.

K220485Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)K183545Anspach Helix Dissection ToolsK180063OCM-G1 AttachmentK131053ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEMK113476ANSPACH DISSECTION TOOLSK082637CRANIAL PERFORATOR

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Related Devices (Code: BWN)

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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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