K955064 · Elekta Instruments, Inc. · HCH · Oct 17, 1996 · Neurology
Device Facts
Record ID
K955064
Device Name
SPETZLER TI 100 ANEURYSM CLIP
Applicant
Elekta Instruments, Inc.
Product Code
HCH · Neurology
Decision Date
Oct 17, 1996
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 882.5200
Device Class
Class 2
Attributes
Therapeutic
Indications for Use
The Spetzler Ti 100 Aneurysm Clips are intended for: - Temporary occlusion of intracranial blood vessels/aneurysms - Permanent placement in the brain for occlusion of intracranial aneurysms
Device Story
Spetzler Ti 100 Aneurysm Clips are surgical implants used for temporary or permanent occlusion of intracranial aneurysms. Manufactured from Grade IV commercially pure titanium (ASTM F67-89), the clips are available in various styles and sizes to accommodate different aneurysm morphologies. They are applied by neurosurgeons using specialized titanium nitride-coated clip appliers to prevent foreign metal transfer. The device is supplied non-sterile and must be sterilized by the user in a dedicated tray prior to each procedure. By utilizing titanium, the device offers improved compatibility with MRI and CT imaging compared to traditional cobalt-chrome alloy clips, resulting in significantly reduced image artifacts and minimal magnetic field interaction. This allows for better visualization of surrounding brain structures in post-operative imaging, potentially aiding clinical decision-making and patient follow-up.
Clinical Evidence
No human clinical trials were conducted. Evidence consists of bench testing and animal studies. Bench testing included metallurgical analysis, mechanical closing force testing (pulsed >20 million cycles), and sterilization validation. Biocompatibility was assessed via a 6-month rabbit intracranial implant study (n=30) comparing titanium to cobalt-chrome, showing no significant differences in EEG, seizure latency, or behavior. MR/CT safety was validated through comparative studies showing titanium clips have significantly lower magnetic susceptibility and reduced image artifact size (up to 700% smaller) compared to predicate alloys.
Technological Characteristics
Material: Grade IV Commercially Pure Titanium (ASTM F67-89). Principle: Mechanical spring-loaded clip for vascular occlusion. Form factor: Various styles/sizes for intracranial use. Connectivity: None. Sterilization: Steam sterilization (autoclave). No software or electronic components.
Indications for Use
Indicated for temporary or permanent occlusion of intracranial blood vessels or aneurysms in patients requiring neurosurgical intervention.
Regulatory Classification
Identification
An aneurysm clip is a device used to occlude an intracranial aneurysm (a balloonlike sac formed on a blood vessel) to prevent it from bleeding or bursting.
{0}
K955064
# 510(k) Summary of Safety and Effectiveness
OCT 17 1996
# SPETZLER Ti 100 TITANIUM ANEURYSM CLIP
## A. LEGALLY MARKETED PREDICATE DEVICES
The Spetzler Ti 100 Aneurysm Clip is substantially equivalent to the Yasargil Aneurysm Clips as manufactured by Aesculap AG, Tutlingen, Germany (as cleared in K772200, K913765, and K922272), the Sugita Aneurysm Clips as manufactured by Mizuho Ikakogyo Co., Ltd., Japan (as cleared in K791978 and K881911), and the Sundt Slim Line Clip as manufactured by Codman and Shurtleff, Randolph, MA (as cleared in K912456).
## B. DEVICE DESCRIPTION
Spetzler Ti 100 Aneurysm Clips are manufactured from titanium--Certified ASTM F67-89, "Unalloyed Titanium for Surgical Implant Applications, Grade IV" (see ASTM F67-89 specifications). This grade of titanium is often referred to as "Commercially Pure Titanium," or "C. P. Titanium." The basic models are distinguished by their surface finish: natural metallic color for clips intended for permanent implantation, and blue for temporary clips.
Aneurysm Clips, whether those proposed by Elekta or those manufactured or distributed by the sponsors of the predicate devices, are available in a wide variety of styles and sizes in order that all of the sizes and shapes of aneurysms can be treated. The clips are available for both temporary and permanent placement in the brain.
Spetzler Ti 100 Aneurysm Clips are applied with the Elekta Titanium Nitride Coated Clip Appliers to avoid foreign metal transfer. Clips are sterilized in the Elekta Sterilization Tray.
## C. INTENDED USE
The Spetzler Ti 100 Aneurysm Clips are intended for:
- Temporary occlusion of intracranial blood vessels/aneurysms
- Permanent placement in the brain for occlusion of intracranial aneurysms
000044
{1}
There are no differences with respect to the predicate devices for indications for use, target population, or mechanical properties.
The Spetzler Ti 100 Aneurysm Clip is safe for use with magnetic resonance (MR) devices, and produces only minimal image distortion, extending only slightly beyond the physical extent of the device. The demonstration of MR safety and compatibility is discussed below.
The Spetzler Ti 100 Aneurysm Clip is safe for use with CT imaging systems and produces significantly less image artifact than clips made from cobalt-chrome alloys such as Elgiloy (Sugita clip) or Phynox (Yasargil clip). The evaluation of the extent of clip induced artifact in CT imaging is discussed below.
The Spetzler Ti 100 Aneurysm Clip and other currently marketed clips such as the Sugita and Codman clips, are supplied to hospitals in a non-sterile package. Clips are selected for a given application and sterilized prior to use by the user. The validation of Elekta's recommended sterilization procedures is discussed below. No effect of repeated sterilization on the mechanical properties of the Elekta clips was found.
## D. SUBSTANTIAL EQUIVALENCE SUMMARY
The Elekta device has the same intended use and target population as the predicate devices, and has equivalent effectiveness for its intended use. Furthermore, its new technological characteristic--the use of titanium--poses the same type of questions about safety and effectiveness as do the predicate devices.
## E. NON-CLINICAL TESTING
This section summarizes the performance testing that Elekta carried out on the Spetzler Ti 100 Aneurysm Clip. This testing addressed the following issues:
(1) Mechanical and metallurgical tests to validate the structural integrity of the clips,
(2) Mechanical performance tests to demonstrate that the clips meet their specifications,
(3) Testing to validate sterilization recommendations
(4) Biocompatibility testing,
(5) MR safety testing, and
(6) Testing to determine image artifact size for MR and CT imaging.
000045
{2}
# 1. Metallurgical/Structural Testing
Elekta’s specifications and tight controls were validated by the following:
a. Destructive testing of a statistically determined number of clips by the independent metallurgical laboratory, Laboratory Testing, Inc., Dublin, PA. A metallographic examination of the surfaces and cross sections, at 100X and 400X, of all stressed, worked and critical areas showed the complete absences of imperfections and defects such as cracks, voids, etc. Such metallurgical examinations will be conducted on samples from each new titanium wire delivery and each clip production lot.
b. Elekta has confirmed that the relatively low temperature of the hospital sterilization process (270° F) has absolutely no effect on the metallurgical/operational properties of the titanium clip. As distributed today, aneurysm clips are provided to the hospital non-sterile (e.g. as by Sugita and Codman). Selected clips are placed in a sterilizing tray and sterilized prior to each procedure until used. In simulating these events, Elekta sterilized the titanium clips in excess of 100 times and after each ten cycles, opened the clips with the Elekta clip applier to the maximum recommended blade opening distance and then measured the closing force per the draft ASTM standard. The closing force remained consistent for all clips.
c. Though titanium is one of the most corrosion resistant metals, Elekta commissioned a corrosion test on the clips. The results confirm that these titanium clips do not corrode, even under stress. This is further confirmed by Elekta’s review of literature concerning the effects of cerebral fluids on titanium.
d. A Vickers hardness was measured on the worked and unworked areas of the clip wire. The results demonstrated no statistically significant change in hardness.
# 2. Mechanical Performance Testing
In evaluating the measure of closing force, Elekta has followed FDA’s recommendation to use the ASTM proposed test protocol to measure each clip, prior to release for distribution. The closing force is recorded on the clip label and in the history file, by serial number.
CCC046
{3}
To confirm that the Spetzler Ti 100 Aneurysm Clips retain their mechanical performance in simulated use conditions, the following study was carried out:
Clips placed on tubing filled with a 98.6° saline solution were pulsed in excess of twenty million cycles at a pressure in excess of 300 mm Hg. Using colored liquid in the tubing, the results confirm no leakage through the clip, no loss of blade alignment, and the changes in closing forces measured (double blind) never went below the release specifications of competitive clips.
## 3. Sterilization
Elekta has validated its recommended steam sterilization cycles. Furthermore, Elekta has demonstrated that repeated sterilization has no effect on the mechanical properties of the clips.
## 4. Biocompatibility
Because titanium has not been previously cleared for use in the brain in an aneurysm clip, it was incumbent upon Elekta to demonstrate that titanium is not significantly different with respect to biocompatibility properties from the cobalt-chrome alloys currently utilized in the predicate devices. This demonstration of biocompatibility includes the following studies commissioned by Elekta:
A study of the Spetzler Ti 100 Aneurysm Clip implanted in the brains of rabbits addresses the concern that titanium might increase the susceptibility to seizure activity. Elekta commissioned a six-month intracranial, pre-clinical implant study of 30 rabbits, divided into three groups, including 12 implanted with titanium clips, 12 implanted with the presently marketed Yasargil Phynox (cobalt chrome alloy) clips and 6 non-implanted controls. These animals were maintained and monitored for one month (six of both groups) and six months (six of both groups) and the six negative controls. The study evaluated the substantial equivalence of the Elekta titanium clip as compared to the presently marketed Yasargil (Aesculap) clip through daily monitoring, monthly EEG evaluations and Time-to-Induced-Seizure. The results of this evaluation demonstrated the substantial equivalence of the Spetzler Ti 100 Aneurysm Clip as there was no difference in the three groups in function and behavior (as recorded in daily observations), no difference in EEG recordings (30 minutes each), and no statistically significant differences in seizure latency.
The study by von Holst, et al. [Acta Neurochirurgica 56:239-242 (1981)] found that clips made of titanium, silver, and tantalum, and implanted in
000047
{4}
the brains of rabbits, were tolerated quite differently. The implant of titanium showed no evidence of any reaction, while the others showed cytoplasmic pigmentation and reactive gliosis (silver) and local limited pigmentation (tantalum).
The report by A. Ammar, "Tissue Compatibility of Different Intracranial Implant Materials: In-vivo and In-Vitro Studies" [Acta Neurochirurgica 72:45-59 (1984)], compared brain implants of alumina ceramics, hydroxy apatite ceramics, titanium, methylmethacrylate, Surgita aneurysm clip, silicon shunt tube, and lyophilized human dura mater (Lyo-dura). While the non-metalic implants had varying degrees of compatibility, the titanium showed excellent compatibility, while the Surgita showed fair compatibility. The report noted for the titanium implant, "No reaction of brain tissue was observed."
Elekta commissioned a major review of the titanium toxicological literature which concluded that:
- Titanium's lack of inflammatory potential is supported by many studies. The available literature indicates that titanium does not act as an immunotoxicant.
- The scientific literature, which indicates that titanium dioxide is non-mutagenic, and the lack of reported tumors in patients with titanium implants, support the position that titanium is not genotoxic.
- The scientific literature and titanium's satisfactory use in many craniofacial implants suggest that titanium will unlikely cause adverse effects in soft tissue.
- The literature and lack of relevant observations among patients with titanium implants demonstrate that titanium dioxide does not cause adverse effects with chronic exposure and suggest that titanium will not elicit systemic effects.
- The available evidence strongly supports titanium's non-carcinogenicity.
- The limited information available on brain implantation shows that titanium does not elicit histopathology and is not associated with dissolution of the oxide layer.
000048
CCC0-8
{5}
# 5. MR Safety and Compatibility
In response to the risks involved in more powerful MRI systems and the continuing concern for image quality in both MRI and CT, Elekta has completed an extensive, performance evaluation of the titanium aneurysm clips:
a. MR Safety
A study carried out at a university included characterization, mechanical testing and magnetic evaluation of the Elekta titanium, Codman, Aesculap and Sugita clips.
The direct measurement of magnetic susceptibility for these clips showed that the MP35N alloy (Codman) was 5.2 times larger than for Elekta's clip, Phynox alloy (Aesculap) was 17.2 times larger, and Elgiloy (Sugita) was 15.7 times larger. The magnetic force measured in a 2 Tesla magnetic field showed that the force was 14, 35, and 36 times larger for MP35N, Phyunox, and Elgiloy, respectively, than for the Elekta clip. The results of this study demonstrate a significantly lower interaction with the magnetic field for titanium over the other clips, some of which are presently promoted as MRI safe.
Furthermore, this study evaluated the magnetization over a cycle of applied magnetic field from 4 Tesla (T) to 0 T to -4 T to 0 T and finally back to 4 T, with measurements every 0.5 T. The resulting M vs B hysteresis loop would show the extent of ferromagnetism, if any. For the Elekta clip the "hysteresis loop" was a shallow straight line through the origin, indicating no detectable ferromagnetism, only paramagnetism. Since the magnetic susceptibility of the Elekta clip is so small and paramagnetic in nature, the magnetic torque on the Elekta clip would be expected to be very small.
Another study used 1.5, 2.0 and 7.0 Tesla fields to evaluate clip displacement/deflection and image quality of the Sugita, Yasargil (Aesculap) and Elekta titanium clips. The results of this study confirm that in 1.5 and 2.0 Tesla fields the forces applied are not significant but in higher fields the Sugita and Aesculap clips show what is presently considered an unacceptable deflection (in excess of 45°) as compared to the titanium clip. In image quality the Elekta titanium clip was found to be "considerably superior in the vicinity of the clip."
000049
{6}
b. Image artifact in MR and CT Imaging
A study carried out at a university showed significantly reduced artifact, for the titanium clip, in MRI and CT scans. In the MR image, the artifact is a signal void with a thin rim of hyperintensity. This artifact was found to be 7.5 times larger for Elgiloy than Elekta and 6 times larger for Phynox. In CT imaging clips cause a streak artifact or starburst pattern. The relative sizes of these artifacts for Elgiloy, Phynox, and C. P. Titanium (Elekta) were in the ratios, 4:3:1.
The ACTA Neurochirurgica paper, "Titanium Clips in Neurosurgery for the Elimination of Artifacts in Computer Tomography (CT)," H. von Holst, et. al., compares the artifacts caused by various intracranial implant materials with titanium (99% pure) and finds that the titanium is highly resistant to corrosion and does not cause artifacts on CT images.
Observations at St. Vincent's Hospital in Dublin, Ireland of artifacts produced by Elekta (titanium), Sugita and Aesculap clips as seen in various MRI fields, were summarized. In this paper, significant artifacts are seen consistently, in various protocols, in both the Sugita and Aesculap clips. In comparison, only a "slight" artifact is seen in the Elekta titanium clip which gives almost no degradation to the surrounding structures.
"Titanium Aneurysm Clip-Decreased Image Degradation in MRI and CT," Michael J. Carron, M.D., et al., presents Dr. Carron's (Southwest Regional Hospital, Florida) imaging evaluations of the Sugita, Aesculap and the Elekta titanium clips in both CT and MRI which were done with regard to three areas: type of artifact, relative size of artifact, degree of degradation of image. The results indicate MRI artifact size 600% to 700% greater for Sugita and Aesculap clips, with significant image degradation, as compared to the Elekta titanium clip. CT artifact is 300% to 400% greater for the Sugita and Aesculap clips with equivalent image degradation while the titanium clip was noted as having no image degradation.
Another study commissioned by Elekta studied image artifact in a dog model, comparing the Spetzler Ti 100 Aneurysm Clip with a Yasargil Phynox alloy clip (Aesculap) of the same size. The main findings were:
- Computed Tomography: Artifact radius of titanium clip measured at 1 cm versus 3 cm for conventional clip.
000050
{7}
- Magnetic Resonance: Artifact dimension in T1, T2 and intermediate weighted images were measured at 0.4 to 1.2 cm² for titanium while conventional clips were at 1.0 to 3.6 cm².
F. CONCLUSIONS
Elekta has demonstrated that its testing of the Spetzler Ti 100 Aneurysm Clip and its review of the literature on the biocompatibility of titanium shows equivalent safety and effectiveness with respect to mechanical performance and biocompatibility issues, and superior performance with respect to the ancillary issues of safety and compatibility with MR and CT imaging systems.
000051
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.