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FDA 510(k)

SNAP STERNUM SAW

K-Number: K935517 · 1994-03-10

ApplicantSurgiquip, Inc.
Decision Date1994-03-10
Product CodeHAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SNAP STERNUM SAW is the device name listed in this FDA 510(k) record. The listed applicant is Surgiquip, Inc.. It received FDA 510(k) clearance on 1994-03-10 under 510(k) number K935517. The device is classified under product code HAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP STERNUM SAW?

SNAP STERNUM SAW is a medical device that received FDA 510(k) clearance on 1994-03-10. The listed applicant is Surgiquip, Inc.. The 510(k) number is K935517.

When did SNAP STERNUM SAW receive FDA 510(k) clearance?

SNAP STERNUM SAW received FDA 510(k) clearance on 1994-03-10, under 510(k) number K935517.

Who is the listed applicant for SNAP STERNUM SAW?

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

What is the FDA product code for SNAP STERNUM SAW?

The FDA product code for SNAP STERNUM SAW is HAB.

Related Clinical Trials

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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Other records listing Surgiquip, 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.

K935322SNAP BONE REAMERK935357SNAP RECIPROCATING SAWK935516SNAP DRILLK931769SNAP OSCILLATING SAW

Related Devices (Code: HAB)

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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