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FDA 510(k)

BONE SAW BLADES

K-Number: K931176 · 1994-01-26

ApplicantBetzler Mfg., Inc.
Decision Date1994-01-26
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BONE SAW BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Betzler Mfg., Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K931176. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE SAW BLADES?

BONE SAW BLADES is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Betzler Mfg., Inc.. The 510(k) number is K931176.

When did BONE SAW BLADES receive FDA 510(k) clearance?

BONE SAW BLADES received FDA 510(k) clearance on 1994-01-26, under 510(k) number K931176.

Who is the listed applicant for BONE SAW BLADES?

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

What is the FDA product code for BONE SAW BLADES?

The FDA product code for BONE SAW BLADES is HWE.

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Related Devices (Code: HWE)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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