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The PAJUNK DeltaCut blopsy system is intended for obtaining biopsies from soft tissues ans soft tissue tumors. It is not appropriate for bone blopsies. The single use, sterile, seperately packaged DeltaCut cannulas are available seperately.

The PAJUNK DeltaCut blopsy system consists of a gun and a disposable cannula. It is intended for obtaining biopsies from soft tissues and soft tissue turnors. It is not appropriate for bone biopsies.

The Pajunk DeltaCut blopsy cannulas are single use sterile devices. They are intended for obtaining biopsies from soft tissues and soft tissue tumors. They are only to be used in combination with the DeltaCut biopsy gun, but they are available seperately. It is not appropriate for bone biopsies.

DeltaCut consist of a non-sterile biopsy gun and a sterile biopsy cannula. The PAJUNK DettaCut biopsy gun is a reusable, spring-loaded, core biopsy device. It features adjustable penetration depths of 15 mm to 22 mm and is sold non-sterlie (see directions for cleaning, sterilization and lubrication). The Pajunk DeltaCut biopsy needle is a disposable needle intended for single use with the Pajunk DeltaCut biopsy gun. The DeltaCut biopsy needle is packaged individually and sterile. It is available in various diameters and lengths. For single patient use. Do not reuse. Do not resterilize. DeltaCut is a cannula system made by Pajunk®, which was developed specifically for the extraction of biopsies from soft tissue. The device is equipped with a visual and mechanical safety-system. Two triggers permit ergonomic handling for right and lefthanded application, regardless of the position of the extraction location. The puncture depth can be adjusted variable on a scale from 15 to 22 mm. The biopsy extraction is carried out in two steps and takes only seconds: 1. First, the inner cannula shoots out forwards and is filled with tissue. 2 Then the cutting cannula instantaneously sildes over it, thereby closing the biopsy chamber and protecting the biopsy material from contamination,

The provided submission for the DeltaCut Biopsy system does not contain specific acceptance criteria or a study that evaluates the device's performance against such criteria. The document is a 510(k) Premarket Notification Submission, focusing on demonstrating substantial equivalence to a predicate device rather than presenting a performance study with detailed acceptance criteria.

The submission confirms the device's intended use, describes its components (biopsy gun and cannula), and highlights its similarity to the Bard® Magnum Biopsy system (K883469), which is the predicate device. It discusses sterilization, packaging, labeling, biocompatibility, and applicable standards (or lack thereof for specific standards for this type of device). The conclusion states that the comparison to predicate devices demonstrates the proposed device is safe, effective, and substantially equivalent.

Therefore, the tables and information requested below cannot be extracted from the provided text as the document does not contain this type of performance study data.

1. A table of acceptance criteria and the reported device performance:
Not available in the provided document. The submission focuses on substantial equivalence to a predicate device, not on meeting specific quantitative performance acceptance criteria in a study.

2. Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective):
Not available in the provided document. There is no performance study described with a test set.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience):
Not available in the provided document.

4. Adjudication method (e.g. 2+1, 3+1, none) for the test set:
Not available in the provided document.

5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:
Not applicable. The DeltaCut Biopsy system is a physical medical device (biopsy gun and cannula), not an AI-assisted diagnostic tool.

6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done:
Not applicable. The DeltaCut Biopsy system is a physical medical device.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.):
Not available in the provided document. There is no performance study described. The document relies on equivalence to a predicate device which is implicitly considered "ground truth" for safety and effectiveness.

8. The sample size for the training set:
Not applicable. This is a physical medical device, not a machine learning algorithm that requires a training set.

9. How the ground truth for the training set was established:
Not applicable. This is a physical medical device.

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The Pajunk insufflation cannula acc. Veress and the modular insufflation cannula acc. Veress is employed in minimal invasive surgery. The cannula is designed for the initial puncture with subsequent gas insuffation for laparoscopic operations. It is used to establish a pneumoperitoneum.

The insufflation cannulae according Veress were developed especially for the safe and efficient r rio moumation oannalae and insufflation cannulae are equipped with maintenance free cocks and a female LuerLock connector. Before application, a sharp outer cannula (sterile packed for modular Veress, reusable for Standard Veress) is mounted onto the reusable inner cannula and fastened by means of a LuerLock connector. Therefore within the modular system , a new, absolutely sharp disposable outer cannula is used for every application. In comparison with totally disposable Veress-cannulae, with the same advantages, the modular system offers a large potential to reduce cost.

This is a premarket notification for a Veress and Modular Veress Insufflation Cannula. This type of submission typically focuses on demonstrating substantial equivalence to a predicate device rather than presenting extensive de novo clinical study data with specific acceptance criteria and detailed device performance metrics. Therefore, many of the requested data points (e.g., sample sizes for test and training sets, number of experts for ground truth, MRMC study details, acceptance criteria table) are not applicable or explicitly provided in this document.

Here's the information that can be extracted or inferred based on the provided text:

1. Table of Acceptance Criteria and Reported Device Performance

This type of information is generally not included in 510(k) submissions for devices like the Veress cannula, which are often cleared based on substantial equivalence to predicate devices rather than meeting specific performance criteria in a new clinical study. The device's performance is assumed to be equivalent to the predicate devices.

2. Sample Size Used for the Test Set and Data Provenance

A formal "test set" in the context of a prospective clinical study with a defined sample size to prove performance against specific acceptance criteria is not described. The submission relies on substantial equivalence and "clinical evaluation and summarizing literature." Therefore, specific sample sizes for a 'test set' derived from a new study are not provided. The data provenance is described as "clinical evaluation and summarizing literature," suggesting a review of existing data rather than a new prospective study.

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts

Not applicable. The submission does not describe a new clinical study with a ground truth established by experts.

4. Adjudication Method for the Test Set

Not applicable. The submission does not describe a new clinical study with an adjudication process.

5. If a Multi Reader Multi Case (MRMC) Comparative Effectiveness Study Was Done, and the Effect Size of How Much Human Readers Improve with AI vs without AI Assistance

Not applicable. This device is a surgical instrument (insufflation cannula), not an AI-powered diagnostic or assistive tool. Therefore, an MRMC study and AI-related metrics are irrelevant.

6. If a Standalone (i.e. algorithm only without human-in-the-loop performance) Was Done

Not applicable. This device is a surgical instrument, not an algorithm.

7. The Type of Ground Truth Used

The "ground truth" for the device's safety and effectiveness is primarily based on substantial equivalence to existing legally marketed predicate devices, which have a history of safe and effective use. Additionally, the submission mentions "clinical evaluation and summarizing literature," suggesting that the medical community's existing knowledge and published findings on similar devices serve as a form of "ground truth" regarding the general principles of Veress cannula use.

8. The Sample Size for the Training Set

Not applicable. This is not an AI/ML device that requires a training set.

9. How the Ground Truth for the Training Set Was Established

Not applicable. This is not an AI/ML device that requires a training set with established ground truth.

Summary of Device Rationale from the Submission:

The submission for the Veress and Modular Veress Insufflation Cannula focuses on demonstrating substantial equivalence to two predicate devices:

1. Cannula with sharp obturator & Veress Needle by Karl Storz (K800668)
2. Veress Cannula et al. by Richard Wolf Medical (K041321)

The rationale provided is that the proposed devices are "as safe and effective as and therefore substantial equivalent to the predicate devices" in terms of intended use, indication, and technical characterization. The document explicitly states: "The comparison between the predicate devices and the proposed devices... demonstrates that the proposed devices are safe and effective, as well as substantially equivalent to the predicate devices." It also mentions "The cannula system acc. Veress has been used for years now. The clinical evaluation and summarizing literature, which is part of this submission (10.0), makes this aspects evident." This implies that prior clinical experience and published data on this type of device support its safety and effectiveness without requiring a new, formal clinical trial with specific performance criteria.

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Pajunk RFTL Radiofrequency needles are electrically insulated and may be used for percutaneous nerve blocks with local anesthetic solution or for radiofrequency lesioning.

Pajunk RFTL Radiofrequency needles are intended for coagulation of soft tissues, such as in long term pain treatment via neurosurgical lesioning procedures, as determined by professional neurosurgeon/ anesthetist and the instructions for use. These RF-cannulas are single use, sterile, non-pyrogenic and latex free medical devices. The RF-cannulas have bevel tips with an active area of 2 - 10 mm.

The needle puncture depth depends on the path chosen by the surgeon to reach and to eliminate the nerve bundle site. This required needle length is the patient contact part of the thermolesion needle. The nerve causing constant pain will be disrupted by utilizing the thermolesion heat radiating from the needle tip. Heat is generated by radio frequency and radiates only from the non-insulated needle tip. This limited heat radiation is used for focussed heat treatment depending on the surgeon's method of operation.

This document is a Premarket Notification Submission (510k) for the Pajunk Thermolesion Cannula "RFTL Radiofrequency Needle". A 510k submission primarily demonstrates substantial equivalence to a predicate device, rather than conducting a de novo study with acceptance criteria and performance reporting as might be expected for a novel device. Therefore, the information provided below will reflect the nature of a 510k submission.

Here is an analysis based on the provided text:

1. Table of Acceptance Criteria and Reported Device Performance

For a 510(k) submission, the "acceptance criteria" are typically demonstrating substantial equivalence to a legally marketed predicate device. The performance is then judged on how well it matches or is considered equivalent to the predicate.

2. Sample Size Used for the Test Set and Data Provenance

This is a 510(k) submission focused on demonstrating substantial equivalence to predicate devices, not on a clinical study that would involve a "test set" in the traditional sense with patient data. Therefore, details regarding a specific sample size for a test set or data provenance (country of origin, retrospective/prospective) are not applicable to this document as no such study is described. The demonstration of equivalence relies on comparing technical characteristics and intended use, not on new clinical performance data from a dedicated test set.

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts

As explained above, no separate "test set" with ground truth established by experts is discussed in this 510(k) submission. Therefore, this information is not applicable. The "ground truth", in a broader sense for a 510(k), is the established safety and effectiveness of the predicate device.

4. Adjudication Method for the Test Set

Again, no "test set" or clinical study requiring an adjudication method is described in this 510(k) submission. This information is not applicable.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done, and the Effect Size

No MRMC comparative effectiveness study is mentioned or implied in this 510(k) submission. This information is not applicable. The submission focuses on device characteristics and equivalence, not on human reader performance with or without AI assistance.

6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) Was Done

This device (a radiofrequency needle) is a physical medical instrument, not an algorithm or AI system. Therefore, the concept of a "standalone algorithm performance" is not applicable. Its use invariably involves a human neurosurgeon/anesthetist.

7. The Type of Ground Truth Used

For a 510(k) submission, the "ground truth" is typically the established safety and effectiveness of the legally marketed predicate devices. The new device aims to be substantially equivalent to this established standard. In this case, the predicate devices are "Radionics thermo lesion needles K021942" and "Stryker's RF cannulas K032406". The comparison also references other Pajunk devices previously cleared by FDA for sterilization and packaging equivalence (K000722, K043130, K033018, K042979, K023218, K013041, K053283).

8. The Sample Size for the Training Set

No "training set" in the context of an algorithm or AI development is mentioned in this document. This information is not applicable.

9. How the Ground Truth for the Training Set Was Established

As no "training set" or AI/algorithm development is described, the method for establishing its "ground truth" is not applicable.

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The Pajunk EpiLong anesthesia conduction kit is indicated for administration of epidural anesthesia.
The Pajunk catheter is placed in the epidural space to facilitate a longer anesthetic effect. After the anesthesia conduction needle has been withdrawn from the patient, the catheter tip can remain in the epidural space for as long as determined by the professional anesthetist and the instructions for use (up to 72 hours).
The Pajunk Loss of Resistance (LOR)-Syringe is intended for use in conjunction with an epidural needle, to verify the needle tip placement in the epidural space by the Loss of Resistance technique as explained in standard medical textbooks. These syringes are not intended for injection or aspiration.
The Pajunk anesthesia conduction flat filter is a microporous filter used while administering to a patient injections of local anesthetics to minimize particulate (foreign material) contamination of the injected fluid.
The Pajunk Tuohy Borst Adaptor is connected to the needle via Luer connector. It ensures sealing and fixation of the catheter end and allows attachment of a Luer Lock syringe or infusion device.

Pajunk's EpiLong set is a single use, sterile, non-pyrogenic and latex free medical device kit. It is a epidural anesthesia kit consisting of a needle for insertion into the epidural space (a special Tuohy Cannula), a catheter for anesthesia administration to the epidural space, a flat filter as well as an adapter. After administration of immediate epidural anesthesia, the epidural catheter may be placed via the cannula into the epidural space. The cannula is then withdrawn, leaving the Epidural Catheter tip in the epidural space for as long as determined by the professional anesthetist and the instructions for use (up to 72 hours).

The provided document is a 510(k) Premarket Notification Submission for the EpiLong Anesthesia Conduction Kit. This type of submission focuses on demonstrating substantial equivalence to a previously legally marketed device (predicate device) rather than proving de novo safety and effectiveness through clinical trials with defined acceptance criteria and performance metrics.

Therefore, the document does not contain the information requested regarding acceptance criteria, study details, sample sizes, expert ground truth, adjudication methods, MRMC studies, standalone performance, or training set specifics.

Instead, the submission states:

• Conclusion: "The comparison between the predicate device and the proposed devices in section 12 of this submission demonstrates that the proposed devices are safe and effective, as well as substantially equivalent to the predicate devices." (Page 1)
• FDA's finding: "We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices..." (Page 2)

In summary, there is no study described in this document that proves acceptance criteria are met, as the regulatory pathway chosen (510(k)) relies on substantial equivalence to a predicate device, not on meeting specific, pre-defined performance acceptance criteria through the types of studies typically associated with AI/software devices.

The document primarily focuses on:

• Device description and indications for use.
• Identification of predicate devices (BBrauns Perifix K813186).
• Mention of sterilization processes.
• A "detailed discussion of substantial equivalence" in a section (Section 12) that is not included in the provided text.

Without Section 12 or other detailed performance testing reports, it's impossible to extract the requested information.

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