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FDA 510(k)

TRANSJAW(TM)

K-Number: K872815 · 1988-01-19

ApplicantVitek, Inc.
Decision Date1988-01-19
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRANSJAW(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Vitek, Inc.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K872815. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSJAW(TM)?

TRANSJAW(TM) is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Vitek, Inc.. The 510(k) number is K872815.

When did TRANSJAW(TM) receive FDA 510(k) clearance?

TRANSJAW(TM) received FDA 510(k) clearance on 1988-01-19, under 510(k) number K872815.

Who is the listed applicant for TRANSJAW(TM)?

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

What is the FDA product code for TRANSJAW(TM)?

The FDA product code for TRANSJAW(TM) is BXB.

Related Clinical Trials

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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