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FDA 510(k)

ANSPACH MENISECTOMY KNIFE

K-Number: K803178 · 1981-02-13

ApplicantThe Anspach Effort, Inc.
Decision Date1981-02-13
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANSPACH MENISECTOMY KNIFE 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 1981-02-13 under 510(k) number K803178. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSPACH MENISECTOMY KNIFE?

ANSPACH MENISECTOMY KNIFE is a medical device that received FDA 510(k) clearance on 1981-02-13. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K803178.

When did ANSPACH MENISECTOMY KNIFE receive FDA 510(k) clearance?

ANSPACH MENISECTOMY KNIFE received FDA 510(k) clearance on 1981-02-13, under 510(k) number K803178.

Who is the listed applicant for ANSPACH MENISECTOMY KNIFE?

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 ANSPACH MENISECTOMY KNIFE?

The FDA product code for ANSPACH MENISECTOMY KNIFE is FZS.

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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: FZS)

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.

K932493SURGICAL CURETTEWhitney Products, Inc.K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDKevtek Medical Products, Inc.K892521CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVECymed, Inc.K891888CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPERZinnanti Surgical Instruments, Inc.K891334ACU-CURETTEAcuderm, Inc.K890366ADENOID CURETTEKinetic Medical Products

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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