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FDA 510(k)

WILLIAMS VERTEBRAL SPREADER

K-Number: K872858 · 1987-10-15

ApplicantAce Medical Co.
Decision Date1987-10-15
Product CodeHXP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WILLIAMS VERTEBRAL SPREADER is the device name listed in this FDA 510(k) record. The listed applicant is Ace Medical Co.. It received FDA 510(k) clearance on 1987-10-15 under 510(k) number K872858. The device is classified under product code HXP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILLIAMS VERTEBRAL SPREADER?

WILLIAMS VERTEBRAL SPREADER is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Ace Medical Co.. The 510(k) number is K872858.

When did WILLIAMS VERTEBRAL SPREADER receive FDA 510(k) clearance?

WILLIAMS VERTEBRAL SPREADER received FDA 510(k) clearance on 1987-10-15, under 510(k) number K872858.

Who is the listed applicant for WILLIAMS VERTEBRAL SPREADER?

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

What is the FDA product code for WILLIAMS VERTEBRAL SPREADER?

The FDA product code for WILLIAMS VERTEBRAL SPREADER is HXP.

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Other records listing Ace Medical Co. 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.

K972183DEPUY ACE A.I.M. TITANIUM TIBIAL NAILK955472ACE HUMERUS & RADIUS PLATESK955388ACE-DUPONT COMPOSITE RINGSK9544856.5MM SOLID CANCELLOUS BONE SCREWK954069ACE CERVICAL TRACTION HALOZS, TONGS & PINSK950618ACE SUPRACONDYLAR PLATE

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Related Devices (Code: HXP)

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.

K800732MENISCOTOMEStainless Mfg., Inc.K800731MENISCAL SAWStainless Mfg., Inc.K800730RETROGRADE KNIFEStainless Mfg., Inc.K800733DOUBLE-EDGE CURETTEStainless Mfg., 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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