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FDA 510(k)

SURGICAL CHISEL

K-Number: K760959 · 1976-11-15

ApplicantAmerican Safety Equipment Corp.
Decision Date1976-11-15
Product CodeEMM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SURGICAL CHISEL is the device name listed in this FDA 510(k) record. The listed applicant is American Safety Equipment Corp.. It received FDA 510(k) clearance on 1976-11-15 under 510(k) number K760959. The device is classified under product code EMM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL CHISEL?

SURGICAL CHISEL is a medical device that received FDA 510(k) clearance on 1976-11-15. The listed applicant is American Safety Equipment Corp.. The 510(k) number is K760959.

When did SURGICAL CHISEL receive FDA 510(k) clearance?

SURGICAL CHISEL received FDA 510(k) clearance on 1976-11-15, under 510(k) number K760959.

Who is the listed applicant for SURGICAL CHISEL?

The FDA 510(k) record lists American Safety Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL CHISEL?

The FDA product code for SURGICAL CHISEL is EMM.

Related Clinical Trials

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Other records listing American Safety Equipment Corp. 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.

K801010KIRSCHNER WIREK771699CARA-STAIN MODEL 3000K760960SURGICAL WIRE DRIVERK760956SURGICAL MICRO DRILLK760958SURGICAL OSCILLATING SAWK760957SURGICAL RECIPROCATING SAW

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Related Devices (Code: EMM)

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.

K963897STERI-OSS SINUS AUGMENTATION KITSteri-Oss, Inc.K864775CHISEL (OSTEOTOME, GOUGE, ETC.)New England Surgical Instrument Corp.K851714820/1 TO 820/51 VARIOUS TYPES BONE RONGEURSArtiberia

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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