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FDA 510(k)

OSTEO COMPRESSION HIP SCREW

K-Number: K920037 · 1992-03-11

ApplicantOsteo AG
Decision Date1992-03-11
Product CodeHRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OSTEO COMPRESSION HIP SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Osteo AG. It received FDA 510(k) clearance on 1992-03-11 under 510(k) number K920037. The device is classified under product code HRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEO COMPRESSION HIP SCREW?

OSTEO COMPRESSION HIP SCREW is a medical device that received FDA 510(k) clearance on 1992-03-11. The listed applicant is Osteo AG. The 510(k) number is K920037.

When did OSTEO COMPRESSION HIP SCREW receive FDA 510(k) clearance?

OSTEO COMPRESSION HIP SCREW received FDA 510(k) clearance on 1992-03-11, under 510(k) number K920037.

Who is the listed applicant for OSTEO COMPRESSION HIP SCREW?

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

What is the FDA product code for OSTEO COMPRESSION HIP SCREW?

The FDA product code for OSTEO COMPRESSION HIP SCREW is HRC.

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Other records listing Osteo AG 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.

K933340OSTEO INTERLOCKING-COMPRESSION NAILK922194OSTEO STEINMANN PINK922195OSTEO FEMORAL NAILK922196OSTEO TIBIA NAILK922193OSTEO KIRSCHNER WIREK920149OSTEO EX-FI-RE

View all 9 devices →

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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