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FDA 510(k)

INTERMEDICS ORTHOPEDICS SAW BLADE

K-Number: K931210 · 1993-11-18

ApplicantIntermedics Orthopedics
Decision Date1993-11-18
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTERMEDICS ORTHOPEDICS SAW BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1993-11-18 under 510(k) number K931210. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERMEDICS ORTHOPEDICS SAW BLADE?

INTERMEDICS ORTHOPEDICS SAW BLADE is a medical device that received FDA 510(k) clearance on 1993-11-18. The listed applicant is Intermedics Orthopedics. The 510(k) number is K931210.

When did INTERMEDICS ORTHOPEDICS SAW BLADE receive FDA 510(k) clearance?

INTERMEDICS ORTHOPEDICS SAW BLADE received FDA 510(k) clearance on 1993-11-18, under 510(k) number K931210.

Who is the listed applicant for INTERMEDICS ORTHOPEDICS SAW BLADE?

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

What is the FDA product code for INTERMEDICS ORTHOPEDICS SAW BLADE?

The FDA product code for INTERMEDICS ORTHOPEDICS SAW BLADE is GFA.

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Related Devices (Code: GFA)

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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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