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FDA 510(k)

CARBIDE CUTTING INSTRUMENT/INTRAARTICU

K-Number: K802598 · 1980-11-19

ApplicantThe Anspach Effort, Inc.
Decision Date1980-11-19
Product CodeHTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CARBIDE CUTTING INSTRUMENT/INTRAARTICU 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 1980-11-19 under 510(k) number K802598. The device is classified under product code HTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBIDE CUTTING INSTRUMENT/INTRAARTICU?

CARBIDE CUTTING INSTRUMENT/INTRAARTICU is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K802598.

When did CARBIDE CUTTING INSTRUMENT/INTRAARTICU receive FDA 510(k) clearance?

CARBIDE CUTTING INSTRUMENT/INTRAARTICU received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802598.

Who is the listed applicant for CARBIDE CUTTING INSTRUMENT/INTRAARTICU?

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 CARBIDE CUTTING INSTRUMENT/INTRAARTICU?

The FDA product code for CARBIDE CUTTING INSTRUMENT/INTRAARTICU is HTT.

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Other records listing The Anspach Effort, Inc. as applicant

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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: HTT)

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.

K862529HALL STERILE BURHall Surgical, Division of Zimmer, Inc.K821695MICRO-AIRE REPLAC. DRILL BURS FOR ZIMMERMicro-Aire Surgical Instruments, Inc.K760236BUR, SURGICAL CARBIDECutter Laboratories, Inc.

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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