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FDA 510(k)

WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)

K-Number: K931037 · 1993-07-30

ApplicantWhitmore Ent., Inc.
Decision Date1993-07-30
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) is the device name listed in this FDA 510(k) record. The listed applicant is Whitmore Ent., Inc.. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K931037. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)?

WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Whitmore Ent., Inc.. The 510(k) number is K931037.

When did WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) receive FDA 510(k) clearance?

WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) received FDA 510(k) clearance on 1993-07-30, under 510(k) number K931037.

Who is the listed applicant for WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)?

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

What is the FDA product code for WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)?

The FDA product code for WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) is FWZ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Whitmore Ent., 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.

K933778WHITMORE ANKLE X-RAY EXTENSION (AXE)

Related Devices (Code: FWZ)

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.

K960019RETRACTOR ARM CLAMPBiopsys Medical, Inc.K945415'LIL MAC ACCESSORY CLAMP(TM)D.L. Nelson and Assoc., Inc.K944779CARBON LIGHTS HAND SURGERY TABLEAllen Medical Systems, Inc.K935381KAPS POSITIONING ARMAndronic Devices, Ltd.K926225SPONGE COUNTERAmerican Medical Manufacturer, Inc.K925035MIDKIFF GEOSTATIC CLAMPD.L. Nelson and Assoc., 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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