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FDA 510(k)

ORTHOPEDIC DRILL GUIDE

K-Number: K871287 · 1987-04-15

ApplicantOrthopedic Systems, Inc.
Decision Date1987-04-15
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC DRILL GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1987-04-15 under 510(k) number K871287. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC DRILL GUIDE?

ORTHOPEDIC DRILL GUIDE is a medical device that received FDA 510(k) clearance on 1987-04-15. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K871287.

When did ORTHOPEDIC DRILL GUIDE receive FDA 510(k) clearance?

ORTHOPEDIC DRILL GUIDE received FDA 510(k) clearance on 1987-04-15, under 510(k) number K871287.

Who is the listed applicant for ORTHOPEDIC DRILL GUIDE?

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

What is the FDA product code for ORTHOPEDIC DRILL GUIDE?

The FDA product code for ORTHOPEDIC DRILL GUIDE is HSZ.

Related Clinical Trials

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Other records listing Orthopedic Systems, 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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910736JACKSON MULTIPURPOSE OPERATING TABLEK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEE

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Related Devices (Code: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, Inc.

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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