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FDA 510(k)

MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT

K-Number: K854887 · 1986-02-28

ApplicantWalter Lorenz Surgical, Inc.
Decision Date1986-02-28
Product CodeEMH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT is the device name listed in this FDA 510(k) record. The listed applicant is Walter Lorenz Surgical, Inc.. It received FDA 510(k) clearance on 1986-02-28 under 510(k) number K854887. The device is classified under product code EMH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT?

MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT is a medical device that received FDA 510(k) clearance on 1986-02-28. The listed applicant is Walter Lorenz Surgical, Inc.. The 510(k) number is K854887.

When did MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT receive FDA 510(k) clearance?

MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT received FDA 510(k) clearance on 1986-02-28, under 510(k) number K854887.

Who is the listed applicant for MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT?

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

What is the FDA product code for MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT?

The FDA product code for MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT is EMH.

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Other records listing Walter Lorenz Surgical, 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.

K063386LORENZ ORTHODONTIC ANCHORAGE SYSTEMK063052LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATESK063506LORENZ STERNAL CLOSURE SYSTEMK062842TWIST DRILLK061384LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUMK042516OTOMIMIX

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Related Devices (Code: EMH)

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.

K890256BONE RONGEUR, DOUBLE-ACTIONKinetic Medical ProductsK890255BONE RONGEUR, SINGLE-ACTIONKinetic Medical ProductsK851710586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORCArtiberiaK834190JAKOBI SURG. INSTRUMENTS #8 15Imm Enterprises , Ltd.K834366SURGICAL INSTRUMENTS & ACCESSORIESC.B.S. Biotechnics, Inc.K821358MODIFIED RONGEURS FOR SPINAL & ORTH. S.Downs Surgical , Ltd.

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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