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FDA 510(k)

MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE

K-Number: K862533 · 1986-08-01

ApplicantWalter Lorenz Surgical, Inc.
Decision Date1986-08-01
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE 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 1986-08-01 under 510(k) number K862533. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE?

MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Walter Lorenz Surgical, Inc.. The 510(k) number is K862533.

When did MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE receive FDA 510(k) clearance?

MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862533.

Who is the listed applicant for MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE?

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 MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE?

The FDA product code for MANUAL SURG. INSTRU. FOR STEINHAUSER BONE PLATE is JEY.

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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: JEY)

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.

K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient SolutionsKLS-Martin L.P.K253206METICULY Patient-specific CMF solutionMeticuly Co., Ltd.K252246Leforte MMF SystemJeil Medical CorporationK253373Southern Craniomaxillofacial (CMF) SystemSouthern Medical (Pty) , Ltd.K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation SystemInion OYK241314KLS Martin Oral-Max Implants MR Conditional (bundled)KLS-Martin L.P.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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